A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585829



Internal ID6973349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41678420..41678744hg38UCSC Ensembl
Innerchr1:41678420..41678744hg38UCSC Ensembl
Outerchr1:41677940..41679127hg38UCSC Ensembl
chr1:42144091..42144415hg19UCSC Ensembl
Innerchr1:42144091..42144415hg19UCSC Ensembl
Outerchr1:42143611..42144798hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9920081, essv9920072, essv9920074, essv9920098, essv9920070, essv9920093, essv9920092, essv9920087, essv9920075, essv9920073, essv9920095, essv9920102, essv9920103, essv9920067, essv9920077, essv9920097, essv9920069, essv9920068, essv9920071, essv9920076, essv9920106, essv9920061, essv9920078, essv9920088, essv9920063, essv9920079, essv9920096, essv9920083, essv9920086, essv9920082, essv9920084, essv9920080, essv9920060, essv9920104, essv9920064, essv9920099, essv9920085, essv9920094, essv9920089, essv9920091, essv9920101, essv9920066, essv9920105, essv9920062, essv9920065, essv9920100, essv9920090
SamplesNA19909, NA19399, HG03057, HG03449, HG02624, HG03193, HG03572, HG03074, HG03436, HG03485, HG03105, NA20291, NA19038, HG02143, HG03212, NA19036, HG03225, HG03583, NA20127, NA19200, HG02009, HG02977, HG03054, HG02450, HG01941, HG03027, HG02470, HG03202, NA18912, HG02585, HG02675, HG02813, HG03240, NA19108, HG02799, HG02759, NA20276, HG02721, HG03469, NA19143, NA19223, HG03077, HG01883, HG02861, NA18505, NA19755, HG03265
Known GenesHIVEP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585829
Frequency
Sample Size2504
Observed Gain0
Observed Loss47
Observed Complex0
Frequencyn/a


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