A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671933



Internal ID9938038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40167498..40215204hg38UCSC Ensembl
Outerchr9:40167127..40215574hg38UCSC Ensembl
Innerchr9:42312516..42360222hg19UCSC Ensembl
Outerchr9:42312145..42360592hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3848448
hg1948448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6430777, essv6028061, essv6055498, essv6324903, essv6189134, essv6484104, essv5561901, essv5835404, essv5887850, essv5534358, essv6101843, essv5971186, essv6522854, essv5521751, essv6377418, essv6029106, essv5441306, essv5693087, essv6225674, essv5444936, essv6418013, essv5777196, essv6370768, essv6059797, essv6575288, essv5532747, essv6427443, essv5802442, essv6409390, essv5668859, essv5442265, essv5789903
SamplesNA20588, NA20761, NA20529, NA20508, NA20783, NA20514, NA20813, NA20802, NA20532, NA20805, NA20586, NA20769, NA20513, NA20518, NA20819, NA20515, NA20535, NA20800, NA20536, NA20770, NA20534, NA20526, NA20799, NA20801, NA20792, NA20504, NA20516, NA20803, NA20797, NA20582, NA20826, NA20528
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671933
Frequency
Sample Size1151
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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