A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691017



Internal ID18989298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:336026..544519hg38UCSC Ensembl
Innerchr9:336026..544519hg19UCSC Ensembl
Innerchr9:326026..534519hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38208494
hg19208494
hg18208494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026342
Supporting Variants
Samples
Known GenesDOCK8, KANK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691017
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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