A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663388



Internal ID15400040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:38936164..38940631hg38UCSC Ensembl
Innerchr8:38793682..38798149hg19UCSC Ensembl
Innerchr8:38912839..38917306hg18UCSC Ensembl
Innerchr8:38912839..38917306hg17UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg384468
hg194468
hg184468
hg174468
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516960
Supporting Variants
Samples
Known GenesPLEKHA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663388
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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