A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519625



Internal ID15446918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:180378226..180389417hg38UCSC Ensembl
Innerchr4:181299379..181310570hg19UCSC Ensembl
Innerchr4:181536373..181547564hg18UCSC Ensembl
Innerchr4:181674528..181685719hg17UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3811192
hg1911192
hg1811192
hg1711192
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696957
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519625
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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