A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680847



Internal ID15070813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18592131..18610735hg38UCSC Ensembl
Innerchr8:18449641..18468245hg19UCSC Ensembl
Innerchr8:18493921..18512525hg18UCSC Ensembl
Innerchr8:18493921..18512525hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3818605
hg1918605
hg1818605
hg1718605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521053
Supporting Variants
Samples
Known GenesPSD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680847
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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