A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067767



Internal ID20634807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43463009..43463120hg38UCSC Ensembl
chr20:42091649..42091760hg19UCSC Ensembl
Cytoband20q13.11
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553176
Supporting Variants
Samples
Known GenesSRSF6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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