A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977256



Internal ID18612462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:67830714..67832672hg38UCSC Ensembl
Innerchr13:68404846..68406804hg19UCSC Ensembl
Innerchr13:67302847..67304805hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg381959
hg191959
hg181959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1968533, nssv1968530, nssv1968535, nssv1968529, nssv1968534, nssv1968532, nssv1968537, nssv1968531, nssv1968538, nssv1968536
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)nsv977256
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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