A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697534



Internal ID15087500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54889804..54940429hg38UCSC Ensembl
Innerchr19:55401170..55451797hg19UCSC Ensembl
Innerchr19:60092982..60143609hg18UCSC Ensembl
Innerchr19:60092982..60143609hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3850626
hg1950628
hg1850628
hg1750628
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520644
Supporting Variants
Samples
Known GenesFCAR, NCR1, NLRP7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697534
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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