A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093397



Internal ID20660437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:124531732..124532159hg38UCSC Ensembl
chr3:124250579..124251006hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369255
Supporting Variants
Samples
Known GenesKALRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093397
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00099


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