A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983580



Internal ID18618773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:41149809..41173713hg38UCSC Ensembl
Innerchr13:41723945..41747849hg19UCSC Ensembl
Innerchr13:40621945..40645849hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3823905
hg1923905
hg1823905
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1961430, nssv1961421, nssv1961427, nssv1961426, nssv1961424, nssv1961422, nssv1961428, nssv1961429, nssv1961423, nssv1961425
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)nsv983580
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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