A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692873



Internal ID15082839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42817913..42961664hg38UCSC Ensembl
Innerchr19:43322065..43465816hg19UCSC Ensembl
Innerchr19:48013905..48157656hg18UCSC Ensembl
Innerchr19:48013905..48157656hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38143752
hg19143752
hg18143752
hg17143752
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG6, PSG7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692873
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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