A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3722893



Internal ID19021174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42782600..42893794hg38UCSC Ensembl
Innerchr19:43286752..43397946hg19UCSC Ensembl
Innerchr19:47978592..48089786hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38111195
hg19111195
hg18111195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059075
Supporting Variants
Samples
Known GenesLOC100289650, PSG1, PSG10P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3722893
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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