A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976135



Internal ID18611342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:76592546..76593155hg38UCSC Ensembl
Innerchr13:77166681..77167290hg19UCSC Ensembl
Innerchr13:76064682..76065291hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38610
hg19610
hg18610
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1970162, nssv1970166, nssv1970163, nssv1970165, nssv1970157, nssv1970160, nssv1970164, nssv1970159, nssv1970158, nssv1970161
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976135
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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