A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519404



Internal ID15446697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13338497..13363857hg38UCSC Ensembl
Innerchr16:13432354..13457714hg19UCSC Ensembl
Innerchr16:13339855..13365215hg18UCSC Ensembl
Innerchr16:13339855..13365215hg17UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3825361
hg1925361
hg1825361
hg1725361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696835
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519404
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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