A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020428



Internal ID20587468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59495472..59495903hg38UCSC Ensembl
chr14:59962190..59962621hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482194
Supporting Variants
Samples
Known GenesJKAMP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020428
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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