A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690092



Internal ID18988373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142409226..142548896hg38UCSC Ensembl
Innerchr8:143490587..143630257hg19UCSC Ensembl
Innerchr8:143488490..143627259hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38139671
hg19139671
hg18138770
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018936
Supporting Variants
Samples
Known GenesBAI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690092
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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