A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665583



Internal ID9931688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151672356..151672841hg38UCSC Ensembl
Outerchr6:151672317..151672898hg38UCSC Ensembl
Innerchr6:151993491..151993976hg19UCSC Ensembl
Outerchr6:151993452..151994033hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6445706, essv6111360, essv5744373, essv5866125, essv6106276, essv6149939, essv6455351, essv6462703, essv6354697, essv6565383, essv6265880, essv5673653, essv6065364, essv5938543, essv5875303, essv5610823, essv5407077, essv5988194, essv6244820, essv6298895, essv6241708, essv6487727, essv5796210, essv6130113, essv5961018, essv5856123, essv5689567, essv5811082, essv6281573, essv6278868, essv5965041, essv5406797, essv5719129, essv5807146, essv5521107, essv6366153, essv6287129, essv5408887, essv6598407, essv5582836
SamplesHG01173, NA12842, HG00249, NA12843, NA20802, NA18545, NA18606, HG00449, NA19443, NA18988, HG00327, NA20796, HG01168, NA20795, NA19062, NA07048, NA19904, NA18611, HG00335, HG00236, NA12889, NA19189, NA18557, NA19789, HG00313, NA12777, HG00380, NA18573, NA12829, NA12249, HG01334, NA20828, NA18536, NA20799, NA19652, NA18533, NA18535, NA19679, NA19726, NA19063
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665583
Frequency
Sample Size1151
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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