A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689700



Internal ID18641295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:89462965..89638067hg38UCSC Ensembl
Innerchr8:90475194..90650295hg19UCSC Ensembl
Innerchr8:90544310..90719411hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38175103
hg19175102
hg18175102
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028969
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)nssv3689700
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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