A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029582



Internal ID21938925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20444693..20444745hg38UCSC Ensembl
chr15:20649946..20649998hg19UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601708
Samples
Known GenesHERC2P3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029582
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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