A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983606



Internal ID18618799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:78761109..78764897hg38UCSC Ensembl
Innerchr13:79335244..79339032hg19UCSC Ensembl
Innerchr13:78233245..78237033hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg383789
hg193789
hg183789
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1970541, nssv1970542, nssv1970536, nssv1970538, nssv1970544, nssv1970540, nssv1970537, nssv1970545, nssv1970539, nssv1970543
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)nsv983606
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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