A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039249



Internal ID20606289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14001634..14119048hg38UCSC Ensembl
chr18:14001633..14119047hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38117415
hg19117415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519072
Supporting Variants
Samples
Known GenesZNF519
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039249
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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