A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984057



Internal ID18619247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41298130..41304074hg38UCSC Ensembl
Innerchr15:41590328..41596272hg19UCSC Ensembl
Innerchr15:39377620..39383564hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg385945
hg195945
hg185945
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2020543, nssv2020544, nssv2020546, nssv2020547, nssv2020541, nssv2020549, nssv2020542, nssv2020540, nssv2020545, nssv2020548
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOIP5-AS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984057
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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