A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984059



Internal ID18619249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42101589..42102089hg38UCSC Ensembl
Innerchr15:42393787..42394287hg19UCSC Ensembl
Innerchr15:40181079..40181579hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2020312, nssv2020314, nssv2020316, nssv2020319, nssv2020313, nssv2020317, nssv2020315, nssv2020321, nssv2020318, nssv2020320
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)nsv984059
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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