A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974093



Internal ID18609306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:52816982..52827933hg38UCSC Ensembl
Innerchr13:53391117..53402068hg19UCSC Ensembl
Innerchr13:52289118..52300069hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3810952
hg1910952
hg1810952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1965086, nssv1965082, nssv1965078, nssv1965084, nssv1965079, nssv1965081, nssv1965087, nssv1965083, nssv1965085, nssv1965080
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)nsv974093
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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