A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655693



Internal ID15045659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8779046..8816277hg38UCSC Ensembl
Innerchr3:8820732..8857963hg19UCSC Ensembl
Innerchr3:8795732..8832963hg18UCSC Ensembl
Innerchr3:8795732..8832963hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3837232
hg1937232
hg1837232
hg1737232
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)nssv655693
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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