A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020477



Internal ID20587517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60146615..60168904hg38UCSC Ensembl
chr14:60613333..60635622hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3822290
hg1922290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485350
Supporting Variants
Samples
Known GenesDHRS7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020477
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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