A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984082



Internal ID18619272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62241646..62242242hg38UCSC Ensembl
Innerchr15:62533845..62534441hg19UCSC Ensembl
Innerchr15:60321137..60321733hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38597
hg19597
hg18597
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2027234, nssv2027233, nssv2027232, nssv2027239, nssv2027236, nssv2027237, nssv2027235, nssv2027240, nssv2027231, nssv2027238
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)nsv984082
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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