A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948105



Internal ID18594951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:83896516..83897236hg38UCSC Ensembl
Innerchr10:85656272..85656992hg19UCSC Ensembl
Innerchr10:85646252..85646972hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38721
hg19721
hg18721
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1858945, nssv1858941, nssv1858943, nssv1858946, nssv1858938, nssv1858947, nssv1858939, nssv1858940, nssv1858944, nssv1858942
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)nsv948105
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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