A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031293



Internal ID21940636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73718252..73718311hg38UCSC Ensembl
chr15:74010593..74010652hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031293
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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