A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068681



Internal ID20635721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15164173..15192869hg38UCSC Ensembl
chr21:16536493..16565189hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3828697
hg1928697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068681
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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