A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648716



Internal ID21840763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39418045..39418779hg38UCSC Ensembl
chr21:40789971..40790705hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043432
Supporting Variants
Samples
Known GenesLCA5L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648716
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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