A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948055



Internal ID18594901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69296255..69311476hg38UCSC Ensembl
Innerchr10:71056011..71071232hg19UCSC Ensembl
Innerchr10:70726017..70741238hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3815222
hg1915222
hg1815222
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1854312, nssv1854315, nssv1854314, nssv1854318, nssv1854311, nssv1854317, nssv1854309, nssv1854316, nssv1854310, nssv1854313
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHK1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948055
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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