A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071999



Internal ID20639039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33916530..33919611hg38UCSC Ensembl
chr21:35288834..35291915hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg383082
hg193082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551730
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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