A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18084592



Internal ID20651632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201544251..201560329hg38UCSC Ensembl
chr2:202408974..202425052hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3816079
hg1916079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6342055
Supporting Variants
Samples
Known GenesALS2CR11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18084592
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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