A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069754



Internal ID20636794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30780972..30790187hg38UCSC Ensembl
chr21:32153290..32162505hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg389216
hg199216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549315
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069754
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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