A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948053



Internal ID18594899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68984349..68984942hg38UCSC Ensembl
Innerchr10:70744105..70744698hg19UCSC Ensembl
Innerchr10:70414111..70414704hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38594
hg19594
hg18594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1853246, nssv1853245, nssv1853244, nssv1853242, nssv1853241, nssv1853239, nssv1853248, nssv1853243, nssv1853247, nssv1853240
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDDX21
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948053
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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