A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027921



Internal ID21937264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40429316..40432097hg38UCSC Ensembl
chr15:40721515..40724296hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382782
hg192782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608817
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027921
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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