A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983578



Internal ID18618771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:40701644..40715044hg38UCSC Ensembl
Innerchr13:41275780..41289180hg19UCSC Ensembl
Innerchr13:40173780..40187180hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3813401
hg1913401
hg1813401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1958894, nssv1958899, nssv1958892, nssv1958897, nssv1958893, nssv1958901, nssv1958896, nssv1958900, nssv1958898, nssv1958895
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)nsv983578
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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