A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029238



Internal ID21938581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93595951..93627103hg38UCSC Ensembl
chr15:94139180..94170332hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3831153
hg1931153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608743
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029238
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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