A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968210



Internal ID18603438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:74877943..74885316hg38UCSC Ensembl
Innerchr5:74173768..74181141hg19UCSC Ensembl
Innerchr5:74209524..74216897hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg387374
hg197374
hg187374
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2365199, nssv2365204, nssv2365201, nssv2365198, nssv2365206, nssv2365197, nssv2365202, nssv2365205, nssv2365200, nssv2365203
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)nsv968210
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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