A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634516



Internal ID21826563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54942705..54942760hg38UCSC Ensembl
chr16:54976617..54976672hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033672
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634516
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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