A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149876



Internal ID15526760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20411600..20610362hg38UCSC Ensembl
Innerchr19:20594407..20793168hg19UCSC Ensembl
Innerchr19:20386247..20585008hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38198763
hg19198762
hg18198762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578832
Supporting Variants
SamplesHGDP00205
Known GenesZNF737, ZNF826P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149876
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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