A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899626



Internal ID15846896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42779968..42889774hg38UCSC Ensembl
Innerchr19:43284120..43393926hg19UCSC Ensembl
Innerchr19:47975960..48085766hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38109807
hg19109807
hg18109807
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579648
Supporting Variants
Samples
Known GenesLOC100289650, PSG1, PSG10P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899626
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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