A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523217



Internal ID21847576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89716146..89721946hg38UCSC Ensembl
chr1:90181705..90187505hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg385801
hg195801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5985220
Supporting Variants
Samples
Known GenesLRRC8C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523217
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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