A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579641



Internal ID16367050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42766413..42857733hg38UCSC Ensembl
Innerchr19:43270565..43361885hg19UCSC Ensembl
Innerchr19:47962405..48053725hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3891321
hg1991321
hg1891321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6461n54
Supporting Variantsnssv899613
Samples
Known GenesLOC100289650, PSG10P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579641
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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