A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017711



Internal ID18760245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36073424..36548245hg38UCSC Ensembl
Innerchr9:36073421..36548242hg19UCSC Ensembl
Innerchr9:36063421..36538242hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38474822
hg19474822
hg18474822
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755933
Samples
Known GenesCCIN, CLTA, GLIPR2, GNE, RECK, RNF38
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017711
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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