A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948204



Internal ID18595050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:119638581..119641737hg38UCSC Ensembl
Innerchr10:121398093..121401249hg19UCSC Ensembl
Innerchr10:121388083..121391239hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg383157
hg193157
hg183157
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1868743, nssv1868749, nssv1868748, nssv1868742, nssv1868744, nssv1868747, nssv1868740, nssv1868745, nssv1868746, nssv1868741
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)nsv948204
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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