A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685342



Internal ID18636937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:21908590..21952074hg38UCSC Ensembl
Innerchr8:21766101..21809585hg19UCSC Ensembl
Innerchr8:21822047..21865531hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3843485
hg1943485
hg1843485
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023009
Supporting Variants
Samples
Known GenesDOK2, XPO7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3685342
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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