A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984019



Internal ID18619209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23322567..23398747hg38UCSC Ensembl
Innerchr15:23567708..23643894hg19UCSC Ensembl
Innerchr15:21119149..21195335hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3876181
hg1976187
hg1876187
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2007233, nssv2007226, nssv2007228, nssv2007231, nssv2007227, nssv2007225, nssv2007230, nssv2007232, nssv2007224, nssv2007229
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGOLGA8S, LOC440243
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984019
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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