A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974068



Internal ID18609281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26236144..26237248hg38UCSC Ensembl
Innerchr13:26810281..26811385hg19UCSC Ensembl
Innerchr13:25708281..25709385hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381105
hg191105
hg181105
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1956435, nssv1956434, nssv1956427, nssv1956429, nssv1956428, nssv1956426, nssv1956433, nssv1956431, nssv1956432, nssv1956430
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)nsv974068
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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