A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948167



Internal ID18248327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100360201..100364192hg38UCSC Ensembl
Innerchr10:102119958..102123949hg19UCSC Ensembl
Innerchr10:102109948..102113939hg18UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg383992
hg193992
hg183992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1866485, nssv1866487, nssv1866481, nssv1866478, nssv1866480, nssv1866486, nssv1866479, nssv1866484, nssv1866483, nssv1866482
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSCD
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948167
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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