A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688667



Internal ID18986948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:53047614..53079271hg38UCSC Ensembl
Innerchr8:53960174..53991831hg19UCSC Ensembl
Innerchr8:54122727..54154384hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3831658
hg1931658
hg1831658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018298
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3688667
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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