A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948142



Internal ID18594988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:93283802..93285717hg38UCSC Ensembl
Innerchr10:95043559..95045474hg19UCSC Ensembl
Innerchr10:95033549..95035464hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg381916
hg191916
hg181916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1865607, nssv1865608, nssv1865613, nssv1865612, nssv1865614, nssv1865609, nssv1865615, nssv1865616, nssv1865611, nssv1865610
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)nsv948142
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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