A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067387



Internal ID20634427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32375820..32377793hg38UCSC Ensembl
chr20:30963623..30965596hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381974
hg191974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531095
Supporting Variants
Samples
Known GenesASXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067387
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00039


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