A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948160



Internal ID18595006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:99012268..99013850hg38UCSC Ensembl
Innerchr10:100772025..100773607hg19UCSC Ensembl
Innerchr10:100762015..100763597hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg381583
hg191583
hg181583
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1865058, nssv1865061, nssv1865062, nssv1865056, nssv1865055, nssv1865059, nssv1865063, nssv1865057, nssv1865060, nssv1865054
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHPSE2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948160
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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