A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679997



Internal ID15069963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42870449..43133031hg38UCSC Ensembl
Innerchr19:43374601..43637183hg19UCSC Ensembl
Innerchr19:48066441..48329023hg18UCSC Ensembl
Innerchr19:48066441..48329023hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38262583
hg19262583
hg18262583
hg17262583
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesPSG1, PSG11, PSG2, PSG6, PSG7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679997
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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