A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608212



Internal ID6995142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17438020..17441680hg38UCSC Ensembl
Innerchr6:17438020..17441680hg38UCSC Ensembl
Outerchr6:17437710..17442075hg38UCSC Ensembl
chr6:17438251..17441911hg19UCSC Ensembl
Innerchr6:17438251..17441911hg19UCSC Ensembl
Outerchr6:17437941..17442306hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383661
hg193661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12204193, essv12204159, essv12204156, essv12204200, essv12204174, essv12204100, essv12204094, essv12204195, essv12204150, essv12204138, essv12204188, essv12204125, essv12204192, essv12204198, essv12204194, essv12204137, essv12204121, essv12204107, essv12204157, essv12204128, essv12204092, essv12204190, essv12204120, essv12204146, essv12204201, essv12204109, essv12204179, essv12204202, essv12204165, essv12204115, essv12204184, essv12204163, essv12204116, essv12204111, essv12204162, essv12204127, essv12204186, essv12204164, essv12204182, essv12204166, essv12204151, essv12204089, essv12204096, essv12204204, essv12204189, essv12204139, essv12204123, essv12204183, essv12204095, essv12204185, essv12204099, essv12204172, essv12204153, essv12204135, essv12204091, essv12204133, essv12204136, essv12204160, essv12204114, essv12204141, essv12204104, essv12204175, essv12204178, essv12204148, essv12204158, essv12204167, essv12204149, essv12204131, essv12204187, essv12204130, essv12204177, essv12204152, essv12204103, essv12204205, essv12204140, essv12204191, essv12204105, essv12204161, essv12204112, essv12204118, essv12204145, essv12204124, essv12204126, essv12204119, essv12204113, essv12204098, essv12204170, essv12204196, essv12204134, essv12204144, essv12204173, essv12204110, essv12204171, essv12204101, essv12204180, essv12204199, essv12204147, essv12204203, essv12204132, essv12204093, essv12204154, essv12204102, essv12204168, essv12204129, essv12204181, essv12204117, essv12204090, essv12204106, essv12204197, essv12204143, essv12204155, essv12204142, essv12204097, essv12204122, essv12204176, essv12204169, essv12204108
SamplesNA18620, HG03514, HG00626, HG02339, HG00650, HG00442, HG03121, HG01965, HG02583, HG03052, NA18507, NA18881, NA18641, HG02836, NA18917, NA19092, HG02870, HG03280, HG03190, HG03515, HG00179, HG01809, HG03199, HG03572, HG03099, HG02595, NA18619, HG00610, NA19384, NA20291, NA19383, HG02315, NA19207, NA19075, NA19087, NA20845, HG03380, HG02073, HG03073, NA20342, NA19025, NA20127, NA18908, HG03832, HG00560, NA19210, HG03132, NA18525, HG01247, NA19462, NA19347, HG03291, HG01879, NA19236, NA18516, NA19982, HG02450, HG01989, NA19081, NA21098, HG03159, HG02537, NA18548, HG00740, HG01392, NA19114, NA18626, HG03388, NA18856, HG03446, HG02881, HG03046, NA19225, HG02586, HG03109, HG02484, HG03567, HG02613, NA18533, NA20276, HG02721, HG01800, NA20362, HG00631, HG03433, HG03127, NA19428, HG02839, NA18943, HG03557, HG03419, HG02814, HG02019, HG03084, HG02771, NA20357, HG02971, HG00478, HG02970, HG01912, HG03097, HG03049, HG03351, NA19116, HG03470, HG03401, HG00728, HG02052, HG01883, NA19129, NA18488, HG03376, HG02465, HG03072, HG02284, HG02629, NA19429
Known GenesCAP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608212
Frequency
Sample Size2504
Observed Gain0
Observed Loss117
Observed Complex0
Frequencyn/a


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