A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694859



Internal ID15431511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96466710..96578536hg38UCSC Ensembl
Innerchr3:96185554..96297380hg19UCSC Ensembl
Innerchr3:97668244..97780070hg18UCSC Ensembl
Innerchr3:97668244..97780070hg17UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38111827
hg19111827
hg18111827
hg17111827
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522087
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694859
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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