A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035818



Internal ID21945161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87614289..87614437hg38UCSC Ensembl
chr16:87647895..87648043hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621478
Samples
Known GenesJPH3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035818
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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