A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948166



Internal ID18248326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100248352..100249449hg38UCSC Ensembl
Innerchr10:102008109..102009206hg19UCSC Ensembl
Innerchr10:101998099..101999196hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg381098
hg191098
hg181098
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1866388, nssv1866386, nssv1866385, nssv1866387, nssv1866383, nssv1866382, nssv1866389, nssv1866384, nssv1866381, nssv1866390
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCWF19L1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948166
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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