A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698971



Internal ID15088937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43001832..43125421hg38UCSC Ensembl
Innerchr19:43505984..43629573hg19UCSC Ensembl
Innerchr19:48197824..48321413hg18UCSC Ensembl
Innerchr19:48197824..48321413hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38123590
hg19123590
hg18123590
hg17123590
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesPSG11, PSG2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698971
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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