A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697527



Internal ID18995808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:84085707..84129560hg38UCSC Ensembl
Innerchr9:86700622..86744475hg19UCSC Ensembl
Innerchr9:85890442..85934295hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3843854
hg1943854
hg1843854
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050840
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3697527
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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