A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976878



Internal ID18612084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20435745..20470952hg38UCSC Ensembl
Innerchr15:20640998..20676205hg19UCSC Ensembl
Innerchr15:18901012..18936219hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3835208
hg1935208
hg1835208
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2003639, nssv2003646, nssv2003640, nssv2003644, nssv2003643, nssv2003638, nssv2003641, nssv2003647, nssv2003645, nssv2003642
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHERC2P3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976878
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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