A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948035



Internal ID18594881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:63902146..63903356hg38UCSC Ensembl
Innerchr10:65661906..65663116hg19UCSC Ensembl
Innerchr10:65331912..65333122hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381211
hg191211
hg181211
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1854077, nssv1854073, nssv1854079, nssv1854076, nssv1854074, nssv1854072, nssv1854075, nssv1854071, nssv1854078, nssv1854070
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)nsv948035
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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