A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699346



Internal ID15435998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145716152..145764299hg38UCSC Ensembl
Innerchr3:145433939..145482086hg19UCSC Ensembl
Innerchr3:146916629..146964776hg18UCSC Ensembl
Innerchr3:146916637..146964784hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3848148
hg1948148
hg1848148
hg1748148
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523565
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699346
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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