A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020596



Internal ID20587636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69460617..69470028hg38UCSC Ensembl
chr14:69927334..69936745hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg389412
hg199412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493442
Supporting Variants
Samples
Known GenesSLC39A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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