A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150131



Internal ID15533114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20651291..20804744hg38UCSC Ensembl
Innerchr19:20834097..20987550hg19UCSC Ensembl
Innerchr19:20625937..20779390hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38153454
hg19153454
hg18153454
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578931
Supporting Variants
SamplesNINDS_110
Known GenesZNF626
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150131
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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