A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18082986



Internal ID20650026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206941801..206942500hg38UCSC Ensembl
chr2:207806525..207807224hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343585
Supporting Variants
Samples
Known GenesCPO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18082986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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