A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948180



Internal ID18595026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:109795445..109818889hg38UCSC Ensembl
Innerchr10:111555203..111578647hg19UCSC Ensembl
Innerchr10:111545193..111568637hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3823445
hg1923445
hg1823445
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1867407, nssv1867415, nssv1867410, nssv1867411, nssv1867406, nssv1867409, nssv1867414, nssv1867408, nssv1867412, nssv1867413
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)nsv948180
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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