A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976942



Internal ID18612148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62244704..62252437hg38UCSC Ensembl
Innerchr15:62536903..62544636hg19UCSC Ensembl
Innerchr15:60324195..60331928hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg387734
hg197734
hg187734
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2027863, nssv2027861, nssv2027857, nssv2027858, nssv2027864, nssv2027856, nssv2027859, nssv2027860, nssv2027862, nssv2027865
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)nsv976942
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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