A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948207



Internal ID18595053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121132933..121133860hg38UCSC Ensembl
Innerchr10:122892447..122893374hg19UCSC Ensembl
Innerchr10:122882437..122883364hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38928
hg19928
hg18928
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1869037, nssv1869031, nssv1869032, nssv1869036, nssv1869034, nssv1869035, nssv1869029, nssv1869033, nssv1869030, nssv1869038
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)nsv948207
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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