A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974072



Internal ID18609285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:28211512..28215918hg38UCSC Ensembl
Innerchr13:28785649..28790055hg19UCSC Ensembl
Innerchr13:27683649..27688055hg18UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg384407
hg194407
hg184407
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1957814, nssv1957812, nssv1957815, nssv1957816, nssv1957813, nssv1957811, nssv1957810, nssv1957818, nssv1957809, nssv1957817
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPAN3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974072
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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