A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029419



Internal ID21938762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58902255..58902479hg38UCSC Ensembl
chr15:59194454..59194678hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599216
Samples
Known GenesSLTM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029419
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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