A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046914



Internal ID19136133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63770336..63845410hg38UCSC Ensembl
Innerchr13:64344469..64419543hg19UCSC Ensembl
Innerchr13:63242470..63317544hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3875075
hg1975075
hg1875075
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1692n100
Supporting Variantsnssv3526791, nssv3526792
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)nsv1046914
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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