A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039084



Internal ID21948427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68831873..68831940hg38UCSC Ensembl
chr15:69124212..69124279hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606925
Samples
Known GenesMIR548H4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039084
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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