A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689732



Internal ID18988013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:94544147..94558305hg38UCSC Ensembl
Innerchr8:95556375..95570533hg19UCSC Ensembl
Innerchr8:95625551..95639709hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3814159
hg1914159
hg1814159
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033345
Supporting Variants
Samples
Known GenesKIAA1429
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689732
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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