A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964860



Internal ID18600096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:62214685..62252426hg38UCSC Ensembl
Innerchr5:61510512..61548253hg19UCSC Ensembl
Innerchr5:61546269..61584010hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3837742
hg1937742
hg1837742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2357903, nssv2357910, nssv2357902, nssv2357905, nssv2357904, nssv2357908, nssv2357906, nssv2357907, nssv2357909, nssv2357911
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)nsv964860
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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