A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069996



Internal ID20637036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:22126417..22277811hg38UCSC Ensembl
chr21:23498736..23650131hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38151395
hg19151396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540071
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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