A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523391



Internal ID18474986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:40222098..40371437hg38UCSC Ensembl
Innerchr13:40796235..40945574hg19UCSC Ensembl
Innerchr13:39694235..39843574hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38149340
hg19149340
hg18149340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046983
Supporting Variants
Samples
Known GenesLINC00598
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3523391
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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