A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035269



Internal ID21944612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65801949..65802129hg38UCSC Ensembl
chr15:66094287..66094467hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035269
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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