A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038266



Internal ID21947609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85015391..85025451hg38UCSC Ensembl
chr16:85048997..85059057hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3810061
hg1910061
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633267
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038266
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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