A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021450



Internal ID20588490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74178914..74186855hg38UCSC Ensembl
chr14:74645617..74653558hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg387942
hg197942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493708
Supporting Variants
Samples
Known GenesLIN52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021450
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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