A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18082975



Internal ID20650015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206768883..206769951hg38UCSC Ensembl
chr2:207633607..207634675hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg381069
hg191069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353076
Supporting Variants
Samples
Known GenesFASTKD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18082975
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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