A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983570



Internal ID18618763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:28778864..28779364hg38UCSC Ensembl
Innerchr13:29353001..29353501hg19UCSC Ensembl
Innerchr13:28251001..28251501hg18UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1957419, nssv1957422, nssv1957417, nssv1957415, nssv1957423, nssv1957418, nssv1957421, nssv1957420, nssv1957416, nssv1957424
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)nsv983570
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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