A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016800



Internal ID20583840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24200610..24205472hg38UCSC Ensembl
chr14:24669816..24674678hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg384863
hg194863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480947
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016800
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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