A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519673



Internal ID15446966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13507020..13522548hg38UCSC Ensembl
Innerchr3:13548520..13564048hg19UCSC Ensembl
Innerchr3:13523520..13539048hg18UCSC Ensembl
Innerchr3:13523520..13539048hg17UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3815529
hg1915529
hg1815529
hg1715529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684600, nssv680975, nssv698802, nssv685602, nssv680213, nssv675314, nssv658213, nssv657667, nssv657501, nssv688343
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519673
Frequency
Sample Size2026
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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