A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984018



Internal ID18619208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22576444..22585136hg38UCSC Ensembl
Innerchr15:23287960..23296652hg19UCSC Ensembl
Innerchr15:20839401..20848093hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg388693
hg198693
hg188693
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2006950, nssv2006945, nssv2006948, nssv2006952, nssv2006951, nssv2006944, nssv2006949, nssv2006946, nssv2006953, nssv2006947
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHERC2P2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984018
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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