A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948205



Internal ID18595051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:119991675..119997472hg38UCSC Ensembl
Innerchr10:121751187..121756984hg19UCSC Ensembl
Innerchr10:121741177..121746974hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg385798
hg195798
hg185798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1868839, nssv1868838, nssv1868840, nssv1868836, nssv1868844, nssv1868835, nssv1868837, nssv1868842, nssv1868843, nssv1868841
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)nsv948205
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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