A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976108



Internal ID18611315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:41420316..41443676hg38UCSC Ensembl
Innerchr13:41994452..42017812hg19UCSC Ensembl
Innerchr13:40892452..40915812hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3823361
hg1923361
hg1823361
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1962152, nssv1962148, nssv1962149, nssv1962150, nssv1962143, nssv1962145, nssv1962147, nssv1962144, nssv1962146, nssv1962151
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR7E37P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976108
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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