A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976945



Internal ID18612151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67985095..67986648hg38UCSC Ensembl
Innerchr15:68277433..68278986hg19UCSC Ensembl
Innerchr15:66064487..66066040hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381554
hg191554
hg181554
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2029793, nssv2029794, nssv2029790, nssv2029791, nssv2029796, nssv2029792, nssv2029799, nssv2029795, nssv2029797, nssv2029798
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)nsv976945
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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