A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697346



Internal ID15087312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:92648479..92669080hg38UCSC Ensembl
Innerchr8:93660707..93681308hg19UCSC Ensembl
Innerchr8:93729883..93750484hg18UCSC Ensembl
Innerchr8:93729883..93750484hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3820602
hg1920602
hg1820602
hg1720602
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520319
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697346
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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