A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947799



Internal ID18594646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28997973..28999877hg38UCSC Ensembl
Innerchr10:29286902..29288806hg19UCSC Ensembl
Innerchr10:29326908..29328812hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg381905
hg191905
hg181905
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1837895, nssv1837893, nssv1837897, nssv1837900, nssv1837892, nssv1837898, nssv1837899, nssv1837896, nssv1837894, nssv1837891
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)nsv947799
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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