A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948032



Internal ID18594878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:60684175..60685175hg38UCSC Ensembl
Innerchr10:62443933..62444933hg19UCSC Ensembl
Innerchr10:62113939..62114939hg18UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1852648, nssv1852644, nssv1852642, nssv1852647, nssv1852640, nssv1852639, nssv1852646, nssv1852645, nssv1852641, nssv1852643
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANK3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948032
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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