A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072773



Internal ID20639813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40745751..40746155hg38UCSC Ensembl
chr21:42117677..42118081hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543199
Supporting Variants
Samples
Known GenesDSCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072773
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00087


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