A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696085



Internal ID18994366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63968448..64617909hg38UCSC Ensembl
Innerchr9:69186118..69630327hg19UCSC Ensembl
Innerchr9:68475938..68920147hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38649462
hg19444210
hg18444210
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022158
Supporting Variants
Samples
Known GenesANKRD20A4, CBWD5, CBWD6, FOXD4L6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696085
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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