A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976951



Internal ID18612157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75186434..75188773hg38UCSC Ensembl
Innerchr15:75478775..75481114hg19UCSC Ensembl
Innerchr15:73265828..73268167hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg382340
hg192340
hg182340
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2031870, nssv2031872, nssv2031878, nssv2031876, nssv2031871, nssv2031873, nssv2031877, nssv2031875, nssv2031879, nssv2031874
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)nsv976951
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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