A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045809



Internal ID18788340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:111027559..111108961hg38UCSC Ensembl
Innerchr13:111679906..111761308hg19UCSC Ensembl
Innerchr13:110477907..110559309hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3881403
hg1981403
hg1881403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1742n100
Supporting Variantsnssv3525601, nssv3525598, nssv3713318, nssv3525600, nssv3525599
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)nsv1045809
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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