A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984073



Internal ID18619263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55181349..55182762hg38UCSC Ensembl
Innerchr15:55473547..55474960hg19UCSC Ensembl
Innerchr15:53260839..53262252hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381414
hg191414
hg181414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2025504, nssv2025501, nssv2025507, nssv2025508, nssv2025499, nssv2025500, nssv2025506, nssv2025502, nssv2025505, nssv2025503
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRSL24D1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984073
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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