A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18070452



Internal ID20637492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56831188..56853242hg38UCSC Ensembl
chr20:55406244..55428298hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3822055
hg1922055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539957
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18070452
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00056


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