A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659610



Internal ID15049576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42897784..43035037hg38UCSC Ensembl
Innerchr19:43401936..43539189hg19UCSC Ensembl
Innerchr19:48093776..48231029hg18UCSC Ensembl
Innerchr19:48093776..48231029hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38137254
hg19137254
hg18137254
hg17137254
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesPSG11, PSG6, PSG7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659610
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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