A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653002



Internal ID15042968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8779054..8836312hg38UCSC Ensembl
Innerchr3:8820740..8877996hg19UCSC Ensembl
Innerchr3:8795740..8852996hg18UCSC Ensembl
Innerchr3:8795740..8852996hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3857259
hg1957257
hg1857257
hg1757257
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)nssv653002
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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