A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703628



Internal ID15093594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18819011..18821047hg38UCSC Ensembl
Innerchr8:18676521..18678557hg19UCSC Ensembl
Innerchr8:18720801..18722837hg18UCSC Ensembl
Innerchr8:18720801..18722837hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg382037
hg192037
hg182037
hg172037
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527228
Supporting Variants
Samples
Known GenesPSD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703628
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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