A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636149



Internal ID21828196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87693663..87693735hg38UCSC Ensembl
chr16:87727269..87727341hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029641
Supporting Variants
Samples
Known GenesJPH3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636149
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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