A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv896539



Internal ID15843809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20638696..20804744hg38UCSC Ensembl
Innerchr19:20821502..20987550hg19UCSC Ensembl
Innerchr19:20613342..20779390hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38166049
hg19166049
hg18166049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578923
Supporting Variants
Samples
Known GenesZNF626
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv896539
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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