A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690931



Internal ID18989212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:46587..208456hg38UCSC Ensembl
Innerchr9:46587..208456hg19UCSC Ensembl
Innerchr9:36587..198456hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38161870
hg19161870
hg18161870
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029900
Supporting Variants
Samples
Known GenesCBWD1, FOXD4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690931
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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