A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6757n54



Internal ID22774652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33818785..33950910hg38UCSC Ensembl
chr2:34043852..34175977hg19UCSC Ensembl
chr2:33897356..34029481hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38132126
hg19132126
hg18132126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv581332, nsv581335, nsv581333
SamplesHGDP00578, HGDP00588, HGDP00557
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6757n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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