A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948153



Internal ID18594999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:96748275..96753643hg38UCSC Ensembl
Innerchr10:98508032..98513400hg19UCSC Ensembl
Innerchr10:98498022..98503390hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg385369
hg195369
hg185369
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1863410, nssv1863414, nssv1863412, nssv1863415, nssv1863416, nssv1863408, nssv1863413, nssv1863411, nssv1863409, nssv1863417
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)nsv948153
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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