A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696068



Internal ID18994349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69166365..69630327hg19UCSC Ensembl
Innerchr9:68456185..68920147hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg19463963
hg18463963
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019181
Supporting Variants
Samples
Known GenesANKRD20A4, CBWD5, CBWD6, FOXD4L6, LOC440896
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696068
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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