A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2760898



Internal ID10377205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:69248737..69405833hg38UCSC Ensembl
Innerchr4:70114455..70271551hg19UCSC Ensembl
Innerchr4:70149044..70306140hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38157097
hg19157097
hg18157097
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv121e203
Supporting Variantsessv7011183, essv7011176, essv7011214, essv7011097, essv7011141, essv7011174, essv7011152, essv7011109, essv7011124, essv7011063, essv7011129, essv7011091, essv7011069, essv7011079, essv7011193, essv7011110, essv7011138, essv7011075, essv7011168, essv7011084, essv7011194, essv7011170, essv7011206, essv7011208, essv7011126, essv7011074, essv7011102, essv7011068, essv7011065, essv7011121, essv7011096, essv7011094, essv7011213, essv7011128, essv7011199, essv7011205, essv7011172, essv7011120, essv7011171, essv7011212, essv7011218, essv7011116, essv7011088, essv7011164, essv7011143, essv7011148, essv7011180, essv7011085, essv7011154, essv7011146, essv7011117, essv7011210, essv7011113, essv7011203, essv7011139, essv7011157, essv7011087, essv7011179, essv7011099, essv7011178, essv7011108, essv7011107, essv7011181, essv7011130, essv7011105, essv7011169, essv7011163, essv7011149, essv7011182, essv7011175, essv7011147, essv7011090, essv7011119, essv7011195, essv7011131, essv7011098, essv7011191, essv7011202, essv7011067, essv7011136, essv7011190, essv7011132, essv7011140, essv7011187, essv7011185, essv7011209, essv7011072, essv7011217, essv7011114, essv7011161, essv7011158, essv7011064, essv7011173, essv7011165, essv7011145, essv7011204, essv7011201, essv7011196, essv7011093, essv7011071, essv7011073, essv7011095, essv7011184, essv7011081, essv7011070, essv7011207, essv7011112, essv7011103, essv7011167, essv7011162, essv7011106, essv7011198, essv7011125, essv7011080, essv7011134, essv7011150, essv7011123, essv7011159, essv7011135, essv7011083, essv7011086, essv7011127, essv7011142, essv7011118, essv7011151, essv7011192, essv7011137, essv7011153, essv7011104, essv7011076, essv7011197, essv7011160, essv7011156, essv7011092, essv7011215, essv7011186, essv7011101, essv7011082, essv7011115, essv7011216
SamplesRW_0208, RW_0300, RW_0071, RW_0356, RW_0636, RW_0644, RW_0305, RW_0039, RW_0239, RW_0520, RW_0323, RW_0196, RW_0345, RW_0359, RW_0634, RW_0595, RW_0187, RW_0270, RW_0312, RW_0322, RW_0560, RW_0559, RW_0180, RW_0658, RW_0025, RW_0629, RW_0319, RW_0181, RW_0217, RW_0116, RW_0096, RW_0011, RW_0511, RW_0614, RW_0255, RW_0179, RW_0334, RW_0137, RW_0216, RW_0174, RW_0626, RW_0246, RW_0218, RW_0358, RW_0357, RW_0131, RW_0512, RW_0267, RW_0528, RW_0230, RW_0522, RW_0541, RW_0519, RW_0540, RW_0023, RW_0659, RW_0539, RW_0500, RW_0103, RW_0061, RW_0637, RW_0143, RW_0197, RW_0576, RW_0505, RW_0185, RW_0311, RW_0279, RW_0567, RW_0346, RW_0002, RW_0214, RW_0077, RW_0611, RW_0593, RW_0666, RW_0091, RW_0587, RW_0288, RW_0653, RW_0515, RW_0222, RW_0625, RW_0257, RW_0597, RW_0129, RW_0252, RW_0212, RW_0260, RW_0210, RW_0092, RW_0328, RW_0056, RW_0276, RW_0578, RW_0249, RW_0308, RW_0523, RW_0195, RW_0120, RW_0564, RW_0341, RW_0166, RW_0331, RW_0669, RW_0543, RW_0235, RW_0562, RW_0529, RW_0013, RW_0048, RW_0232, RW_0275, RW_0132, RW_0284, RW_0229, RW_0220, RW_0662, RW_0119, RW_0215, RW_0574, RW_0128, RW_0154, RW_0170, RW_0613, RW_0031, RW_0079, RW_0652, RW_0263, RW_0156, RW_0033, RW_0223, RW_0336, RW_0139, RW_0594, RW_0285, RW_0162, RW_0532
Known GenesUGT2B28
MethodMerging
AnalysisTwo different algorithms (PennCNV and Birdseye) were applied to detect CNVs. Only congruent CNV events regarding direction of effect that were detected by both algorithms were merged using the outer borders of the event in a first step. In a second step only CNVs that were detected in at least two individuals were merged into a CNVR.
PlatformMerging
Comments
ReferenceVogler_et_al_2010
Pubmed ID21179565
Accession Number(s)esv2760898
Frequency
Sample Size1109
Observed Gain3
Observed Loss135
Observed Complex0
Frequencyn/a


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