A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691464



Internal ID18989745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:117589866..117627923hg38UCSC Ensembl
Innerchr8:118602105..118640162hg19UCSC Ensembl
Innerchr8:118671286..118709343hg18UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg3838058
hg1938058
hg1838058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028387
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)nssv3691464
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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