A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948107



Internal ID18594953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84387445..84392170hg38UCSC Ensembl
Innerchr10:86147201..86151926hg19UCSC Ensembl
Innerchr10:86137181..86141906hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg384726
hg194726
hg184726
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1859927, nssv1859925, nssv1859931, nssv1859924, nssv1859933, nssv1859930, nssv1859929, nssv1859926, nssv1859928, nssv1859932
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCCSER2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948107
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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