A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18087853



Internal ID20654893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:41852443..41886000hg38UCSC Ensembl
chr2:42079583..42113140hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3833558
hg1933558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350688
Supporting Variants
Samples
Known GenesLOC388942
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18087853
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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