A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18070895



Internal ID20637935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16486245..16491709hg38UCSC Ensembl
chr21:17858565..17864029hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg385465
hg195465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536072
Supporting Variants
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18070895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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