A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18084014



Internal ID20651054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201097801..201099300hg38UCSC Ensembl
chr2:201962524..201964023hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351260
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18084014
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00036


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