A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068802



Internal ID20635842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37757228..37840183hg38UCSC Ensembl
chr20:36385630..36468585hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3882956
hg1982956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522321
Supporting Variants
Samples
Known GenesCTNNBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068802
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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