A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580921



Internal ID16368330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9304713..9305582hg38UCSC Ensembl
Innerchr2:9444842..9445711hg19UCSC Ensembl
Innerchr2:9362293..9363162hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38870
hg19870
hg18870
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv903589
Samples
Known GenesASAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580921
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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