A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3687247



Internal ID18638842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:42093555..42134046hg38UCSC Ensembl
Innerchr8:41951073..41991564hg19UCSC Ensembl
Innerchr8:42070230..42110721hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3840492
hg1940492
hg1840492
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022636
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)nssv3687247
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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