A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671024



Internal ID15060990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8784337..8816277hg38UCSC Ensembl
Innerchr3:8826023..8857963hg19UCSC Ensembl
Innerchr3:8801023..8832963hg18UCSC Ensembl
Innerchr3:8801023..8832963hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3831941
hg1931941
hg1831941
hg1731941
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517310
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671024
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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