A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519072



Internal ID20892433
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 StatusM
Merged Variants
Supporting Variantsnssv18039249
Samples
Known GenesZNF519
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519072
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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