A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657374



Internal ID15394026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2346023..2364872hg38UCSC Ensembl
Innerchr8:2302926..2321764hg19UCSC Ensembl
Innerchr8:2290333..2309171hg18UCSC Ensembl
Innerchr8:2290333..2309171hg17UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg3818850
hg1918839
hg1818839
hg1718839
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515930
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657374
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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