A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691215



Internal ID18989496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1216007..1472056hg38UCSC Ensembl
Innerchr9:1216007..1472056hg19UCSC Ensembl
Innerchr9:1206007..1462056hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38256050
hg19256050
hg18256050
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031506
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)nssv3691215
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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