A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043181



Internal ID18785712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:43182667..43208073hg38UCSC Ensembl
Innerchr13:43756803..43782209hg19UCSC Ensembl
Innerchr13:42654803..42680209hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3825407
hg1925407
hg1825407
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1643n100
Supporting Variantsnssv3714978
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)nsv1043181
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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