A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694439



Internal ID15084405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18617655..18621677hg38UCSC Ensembl
Innerchr8:18475165..18479187hg19UCSC Ensembl
Innerchr8:18519445..18523467hg18UCSC Ensembl
Innerchr8:18519445..18523467hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg384023
hg194023
hg184023
hg174023
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521368
Supporting Variants
Samples
Known GenesPSD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694439
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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