A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022295



Internal ID21931638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85533704..85547782hg38UCSC Ensembl
chr16:85567310..85581388hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3814079
hg1914079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618674
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022295
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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