A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983602



Internal ID18618795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:73114671..73118360hg38UCSC Ensembl
Innerchr13:73688808..73692497hg19UCSC Ensembl
Innerchr13:72586809..72590498hg18UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg383690
hg193690
hg183690
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1968739, nssv1968738, nssv1968735, nssv1968733, nssv1968732, nssv1968740, nssv1968736, nssv1968734, nssv1968741, nssv1968737
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)nsv983602
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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