A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581607



Internal ID16369016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41842158..41974468hg38UCSC Ensembl
Innerchr2:42069298..42201608hg19UCSC Ensembl
Innerchr2:41922802..42055112hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38132311
hg19132311
hg18132311
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150422
SamplesHGDP01078
Known GenesC2orf91, LOC388942
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581607
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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