A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693533



Internal ID15430185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162160925..162231496hg38UCSC Ensembl
Innerchr3:161878713..161949284hg19UCSC Ensembl
Innerchr3:163361407..163431978hg18UCSC Ensembl
Innerchr3:163361415..163431986hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3870572
hg1970572
hg1870572
hg1770572
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516722
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693533
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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