A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962500



Internal ID18597743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14883874..14893208hg38UCSC Ensembl
Innerchr18:14883873..14893207hg19UCSC Ensembl
Innerchr18:14873873..14883207hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg389335
hg199335
hg189335
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv40n82
Supporting Variantsnssv2119414, nssv2119412, nssv2119409, nssv2119413, nssv2119406, nssv2119407, nssv2119411, nssv2119408, nssv2119410, nssv2119405
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)nsv962500
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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