A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18082978



Internal ID20650018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206795066..206799462hg38UCSC Ensembl
chr2:207659790..207664186hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg384397
hg194397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6339767
Supporting Variants
Samples
Known GenesFASTKD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18082978
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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