A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626930



Internal ID7013760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80257345..80275559hg38UCSC Ensembl
Innerchr11:80257845..80275059hg38UCSC Ensembl
Outerchr11:80256345..80276559hg38UCSC Ensembl
chr11:79968389..79986603hg19UCSC Ensembl
Innerchr11:79968889..79986103hg19UCSC Ensembl
Outerchr11:79967389..79987603hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3818215
hg1918215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14216171, essv14216176, essv14216184, essv14216220, essv14216207, essv14216238, essv14216183, essv14216219, essv14216221, essv14216191, essv14216212, essv14216211, essv14216206, essv14216168, essv14216231, essv14216188, essv14216226, essv14216228, essv14216209, essv14216225, essv14216214, essv14216230, essv14216194, essv14216174, essv14216169, essv14216205, essv14216180, essv14216218, essv14216185, essv14216192, essv14216233, essv14216215, essv14216210, essv14216199, essv14216237, essv14216187, essv14216229, essv14216204, essv14216232, essv14216208, essv14216177, essv14216217, essv14216200, essv14216189, essv14216224, essv14216227, essv14216181, essv14216172, essv14216193, essv14216201, essv14216213, essv14216216, essv14216173, essv14216182, essv14216222, essv14216197, essv14216186, essv14216170, essv14216196, essv14216202, essv14216166, essv14216195, essv14216165, essv14216203, essv14216179, essv14216236, essv14216167, essv14216190, essv14216198, essv14216234, essv14216235, essv14216178, essv14216223, essv14216175
SamplesHG02614, NA18502, NA19701, NA19648, HG03484, HG02628, HG03052, HG02702, HG03517, HG04211, HG03449, NA18877, HG02012, NA19092, HG02804, HG03455, HG02895, HG02769, HG03478, HG03074, HG03436, HG02952, NA20320, HG02840, HG03485, HG02620, HG02143, HG03268, HG03045, HG03195, NA19159, HG02427, NA18864, HG03073, HG03058, HG03055, NA18908, NA19707, HG03088, HG02334, HG03547, HG02322, NA19982, HG02887, HG03575, HG03081, HG03027, HG02470, HG03397, NA18856, NA19625, HG02568, HG02722, HG02813, HG03539, NA20362, NA18865, HG03304, HG03557, HG03084, NA18501, HG03039, NA20348, HG03646, HG03097, HG03066, HG03313, NA19713, HG02676, HG02052, HG02629, HG03439, HG02760, HG03741
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626930
Frequency
Sample Size2504
Observed Gain0
Observed Loss74
Observed Complex0
Frequencyn/a


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