A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18124940



Internal ID20691980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:110952584..110998156hg38UCSC Ensembl
chr5:110288283..110333855hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3845573
hg1945573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407613
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18124940
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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