A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947866



Internal ID18594713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38617148..38736281hg38UCSC Ensembl
Innerchr10:38910279..39029412hg19UCSC Ensembl
Innerchr10:38950285..39069418hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38119134
hg19119134
hg18119134
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1842092, nssv1842085, nssv1842090, nssv1842087, nssv1842093, nssv1842094, nssv1842091, nssv1842088, nssv1842086, nssv1842089
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesACTR3BP5
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947866
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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