A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947894



Internal ID18594741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42882535..42894550hg38UCSC Ensembl
Innerchr10:43377983..43389998hg19UCSC Ensembl
Innerchr10:42697989..42710004hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3812016
hg1912016
hg1812016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1845163, nssv1845166, nssv1845172, nssv1845165, nssv1845164, nssv1845170, nssv1845171, nssv1845167, nssv1845169, nssv1845168
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)nsv947894
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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