A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947915



Internal ID18594761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45750267..45769503hg38UCSC Ensembl
Innerchr10:46245715..46264951hg19UCSC Ensembl
Innerchr10:45565721..45584957hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3819237
hg1919237
hg1819237
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1846102, nssv1846098, nssv1846103, nssv1846101, nssv1846105, nssv1846106, nssv1846099, nssv1846107, nssv1846104, nssv1846100
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM21C
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947915
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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