A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521442



Internal ID15448735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:16150636..16172173hg38UCSC Ensembl
Innerchr3:16192143..16213680hg19UCSC Ensembl
Innerchr3:16167147..16188684hg18UCSC Ensembl
Innerchr3:16167147..16188684hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3821538
hg1921538
hg1821538
hg1721538
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698052
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521442
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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