A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18017349



Internal ID20584389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:33499001..33535400hg38UCSC Ensembl
chr14:33968207..34004606hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3836400
hg1936400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482009
Supporting Variants
Samples
Known GenesNPAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18017349
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00054


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