A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685926



Internal ID15075892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42817913..42964508hg38UCSC Ensembl
Innerchr19:43322065..43468660hg19UCSC Ensembl
Innerchr19:48013905..48160500hg18UCSC Ensembl
Innerchr19:48013905..48160500hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38146596
hg19146596
hg18146596
hg17146596
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)nssv685926
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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