A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664056



Internal ID9930161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:24529763..24535112hg38UCSC Ensembl
Outerchr16:24529606..24535265hg38UCSC Ensembl
Innerchr16:24541084..24546433hg19UCSC Ensembl
Outerchr16:24540927..24546586hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg385660
hg195660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv488e199
Supporting Variantsessv6152783, essv5768483, essv5950311, essv6438936, essv6449527, essv5625473, essv6336268, essv5836211, essv5895984, essv6309756, essv6412190, essv5533248, essv6091199, essv5910426, essv6016234, essv6244358, essv6332105, essv6384621, essv5752272, essv5699943, essv5906534, essv5660042, essv5685434, essv6486339, essv6359746, essv5638101, essv5756610, essv5470386, essv5746603, essv6048058, essv6339006, essv5809718, essv5706945, essv5907095, essv5556740, essv6165834, essv6146363
SamplesNA19701, NA19703, NA19397, NA18924, HG01462, NA18486, NA20294, NA19355, NA19377, HG01461, NA19920, NA19107, NA19396, NA19197, NA19404, NA18874, NA19172, NA19901, NA18520, NA20342, NA19445, NA18934, NA19982, NA18853, NA18523, NA19434, NA19835, NA19467, NA19360, NA19818, NA20348, NA19223, NA19102, NA18873, NA19316, NA18522, NA19431
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664056
Frequency
Sample Size1151
Observed Gain0
Observed Loss37
Observed Complex0
Frequencyn/a


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