A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672537



Internal ID9938642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15803087..15804935hg38UCSC Ensembl
chr1:16129582..16131430hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg381849
hg191849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5798425, essv6256469, essv5847534, essv6452740, essv5888075, essv6344540, essv5493439, essv6315106, essv6036373, essv6227263, essv6410505, essv6343216, essv6439037, essv5872941, essv6340165, essv6253229, essv6264811, essv5751674, essv6381980
SamplesNA19092, NA18959, NA19920, HG00261, NA18988, NA19130, NA19172, NA19236, NA20799, NA18950, NA19835, NA20582, NA19060, NA19716, NA19713, NA18873, NA19116, NA19900, NA19004
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672537
Frequency
Sample Size1151
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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