A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046983



Internal ID18789514
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 StatusM
Merged Variantsdgv1633n100
Supporting Variantsnssv3523391
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)nsv1046983
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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