A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622023



Internal ID21814070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71736540..71736752hg38UCSC Ensembl
chr16:71770443..71770655hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022601
Supporting Variants
Samples
Known GenesAP1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622023
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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