A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102224



Internal ID20669264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50549133..50571541hg38UCSC Ensembl
chr3:50586564..50608972hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3822409
hg1922409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358466
Supporting Variants
Samples
Known GenesC3orf18, HEMK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102224
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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