A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948165



Internal ID18595011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100109490..100114331hg38UCSC Ensembl
Innerchr10:101869247..101874088hg19UCSC Ensembl
Innerchr10:101859237..101864078hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg384842
hg194842
hg184842
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1866284, nssv1866288, nssv1866290, nssv1866292, nssv1866291, nssv1866293, nssv1866285, nssv1866286, nssv1866287, nssv1866289
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)nsv948165
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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