A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149850



Internal ID15506559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19910237..20040448hg38UCSC Ensembl
Innerchr19:20021046..20151257hg19UCSC Ensembl
Innerchr19:19882046..20012257hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38130212
hg19130212
hg18130212
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578800
Supporting Variants
Samples1780854017_A
Known GenesZNF682, ZNF93
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149850
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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