A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976962



Internal ID18612168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:88949674..88954262hg38UCSC Ensembl
Innerchr15:89492905..89497493hg19UCSC Ensembl
Innerchr15:87293909..87298497hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg384589
hg194589
hg184589
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2036593, nssv2036601, nssv2036598, nssv2036595, nssv2036599, nssv2036597, nssv2036596, nssv2036594, nssv2036602, nssv2036600
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)nsv976962
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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