A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948149



Internal ID18594995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:96187713..96191391hg38UCSC Ensembl
Innerchr10:97947469..97951147hg19UCSC Ensembl
Innerchr10:97937459..97941137hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg383679
hg193679
hg183679
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1863710, nssv1863719, nssv1863717, nssv1863715, nssv1863711, nssv1863712, nssv1863713, nssv1863718, nssv1863714, nssv1863716
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)nsv948149
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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