A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697522



Internal ID18995803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:83048759..83132647hg38UCSC Ensembl
Innerchr9:85663674..85747562hg19UCSC Ensembl
Innerchr9:84853494..84937382hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3883889
hg1983889
hg1883889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043722
Supporting Variants
Samples
Known GenesRASEF
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3697522
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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