A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976947



Internal ID18265467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69455116..69455768hg38UCSC Ensembl
Innerchr15:69747455..69748107hg19UCSC Ensembl
Innerchr15:67534509..67535161hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38653
hg19653
hg18653
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2030455, nssv2030458, nssv2030464, nssv2030463, nssv2030460, nssv2030456, nssv2030461, nssv2030459, nssv2030457, nssv2030462
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRPLP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976947
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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