A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984060



Internal ID18619250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42579023..42580439hg38UCSC Ensembl
Innerchr15:42871221..42872637hg19UCSC Ensembl
Innerchr15:40658513..40659929hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381417
hg191417
hg181417
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2019734, nssv2019728, nssv2019733, nssv2019732, nssv2019726, nssv2019725, nssv2019729, nssv2019731, nssv2019730, nssv2019727
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSTARD9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984060
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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