A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150412



Internal ID15853865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:21324131..21392468hg38UCSC Ensembl
Innerchr2:21547003..21615340hg19UCSC Ensembl
Innerchr2:21400508..21468845hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3868338
hg1968338
hg1868338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581170
Supporting Variants
Samples1780854464_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150412
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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