A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947806



Internal ID18247967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29585778..29588181hg38UCSC Ensembl
Innerchr10:29874707..29877110hg19UCSC Ensembl
Innerchr10:29914713..29917116hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg382404
hg192404
hg182404
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1837202, nssv1837198, nssv1837203, nssv1837206, nssv1837205, nssv1837199, nssv1837197, nssv1837201, nssv1837200, nssv1837204
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSVIL
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947806
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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