A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701982



Internal ID15438634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:34710497..34757936hg38UCSC Ensembl
Innerchr8:34568015..34615454hg19UCSC Ensembl
Innerchr8:34687557..34734996hg18UCSC Ensembl
Innerchr8:34687557..34734996hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3847440
hg1947440
hg1847440
hg1747440
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525800
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701982
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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