A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv896562



Internal ID15843832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20651291..20807649hg38UCSC Ensembl
Innerchr19:20834097..20990455hg19UCSC Ensembl
Innerchr19:20625937..20782295hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38156359
hg19156359
hg18156359
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578933
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)nssv896562
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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