A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976115



Internal ID18611322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:51906787..51910435hg38UCSC Ensembl
Innerchr13:52480923..52484571hg19UCSC Ensembl
Innerchr13:51378924..51382572hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg383649
hg193649
hg183649
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1963741, nssv1963743, nssv1963744, nssv1963745, nssv1963738, nssv1963739, nssv1963746, nssv1963747, nssv1963740, nssv1963742
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)nsv976115
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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