A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964898



Internal ID18600134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:77576436..77583155hg38UCSC Ensembl
Innerchr5:76872261..76878980hg19UCSC Ensembl
Innerchr5:76908017..76914736hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg386720
hg196720
hg186720
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2366467, nssv2366462, nssv2366466, nssv2366468, nssv2366465, nssv2366469, nssv2366471, nssv2366464, nssv2366470, nssv2366463
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)nsv964898
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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