A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069442



Internal ID20636482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17594689..17595530hg38UCSC Ensembl
chr21:18967007..18967848hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550728
Supporting Variants
Samples
Known GenesBTG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069442
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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