A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964921



Internal ID18600156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:109585762..109589955hg38UCSC Ensembl
Innerchr5:108921463..108925656hg19UCSC Ensembl
Innerchr5:108949362..108953555hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg384194
hg194194
hg184194
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2372328, nssv2372326, nssv2372327, nssv2372324, nssv2372320, nssv2372329, nssv2372325, nssv2372322, nssv2372321, nssv2372323
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)nsv964921
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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