A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948162



Internal ID18595008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:99932186..99935311hg38UCSC Ensembl
Innerchr10:101691943..101695068hg19UCSC Ensembl
Innerchr10:101681933..101685058hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg383126
hg193126
hg183126
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1865861, nssv1865857, nssv1865860, nssv1865862, nssv1865854, nssv1865863, nssv1865859, nssv1865855, nssv1865858, nssv1865856
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDNMBP, DNMBP-AS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948162
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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