A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039254



Internal ID20606294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14071651..14280291hg38UCSC Ensembl
chr18:14071650..14280290hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38208641
hg19208641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519145
Supporting Variants
Samples
Known GenesANKRD20A5P, ZNF519
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039254
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00056


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