A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964899



Internal ID18600135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:77782753..77787388hg38UCSC Ensembl
Innerchr5:77078577..77083212hg19UCSC Ensembl
Innerchr5:77114333..77118968hg18UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg384636
hg194636
hg184636
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2364394, nssv2364385, nssv2364390, nssv2364387, nssv2364391, nssv2364386, nssv2364393, nssv2364389, nssv2364392, nssv2364388
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)nsv964899
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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