A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977684



Internal ID18612890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28673820..28729293hg38UCSC Ensembl
Innerchr15:28918966..28974439hg19UCSC Ensembl
Innerchr15:26718007..26773480hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3855474
hg1955474
hg1855474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2015039, nssv2015043, nssv2015041, nssv2015044, nssv2015040, nssv2015042, nssv2015047, nssv2015038, nssv2015045, nssv2015046
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGOLGA8M, HERC2P9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977684
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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