A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968868



Internal ID18604096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5024419..5032666hg38UCSC Ensembl
Innerchr5:5024532..5032779hg19UCSC Ensembl
Innerchr5:5077532..5085779hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg388248
hg198248
hg188248
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2344079, nssv2344083, nssv2344076, nssv2344081, nssv2344075, nssv2344077, nssv2344084, nssv2344082, nssv2344078, nssv2344080
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)nsv968868
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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