A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085497



Internal ID20652537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219067014..219067581hg38UCSC Ensembl
chr2:219931736..219932303hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337954
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085497
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00469


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