A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517256



Internal ID15097863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20651291..20804744hg38UCSC Ensembl
Innerchr19:20834097..20987550hg19UCSC Ensembl
Innerchr19:20625937..20779390hg18UCSC Ensembl
Innerchr19:20625937..20779390hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38153454
hg19153454
hg18153454
hg17153454
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686464, nssv686022, nssv687665, nssv654133, nssv677612, nssv671810
Samples
Known GenesZNF626
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517256
Frequency
Sample Size2026
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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