A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071693



Internal ID20638733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26309472..26309879hg38UCSC Ensembl
chr21:27681791..27682198hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548975
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00119


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