A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694614



Internal ID15084580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8256540..8287918hg38UCSC Ensembl
Innerchr8:8114062..8145440hg19UCSC Ensembl
Innerchr8:8151472..8182850hg18UCSC Ensembl
Innerchr8:8151472..8182850hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3831379
hg1931379
hg1831379
hg1731379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515968
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694614
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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