A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976908



Internal ID18612114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28624719..28659180hg38UCSC Ensembl
Innerchr15:28869865..28904326hg19UCSC Ensembl
Innerchr15:26668906..26703367hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3834462
hg1934462
hg1834462
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2014898, nssv2014891, nssv2014894, nssv2014895, nssv2014892, nssv2014897, nssv2014896, nssv2014890, nssv2014889, nssv2014893
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHERC2P9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976908
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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