A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691543



Internal ID18989824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131954275..131986465hg38UCSC Ensembl
Innerchr8:132966522..132998712hg19UCSC Ensembl
Innerchr8:133035704..133067894hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3832191
hg1932191
hg1832191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018399
Supporting Variants
Samples
Known GenesEFR3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691543
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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