A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968961



Internal ID18604189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:86301405..86307280hg38UCSC Ensembl
Innerchr5:85597223..85603098hg19UCSC Ensembl
Innerchr5:85632979..85638854hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg385876
hg195876
hg185876
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2368175, nssv2368178, nssv2368174, nssv2368181, nssv2368180, nssv2368183, nssv2368182, nssv2368176, nssv2368177, nssv2368179
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968961
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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