A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069394



Internal ID20636434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17182620..17183060hg38UCSC Ensembl
chr21:18554938..18555378hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550260
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069394
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00092


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