A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947736



Internal ID18594583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:10168481..10177196hg38UCSC Ensembl
Innerchr10:10210444..10219159hg19UCSC Ensembl
Innerchr10:10250450..10259165hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg388716
hg198716
hg188716
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1833123, nssv1833131, nssv1833129, nssv1833125, nssv1833128, nssv1833124, nssv1833127, nssv1833132, nssv1833130, nssv1833126
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947736
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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