A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016707



Internal ID20583747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22859901..22867900hg38UCSC Ensembl
chr14:23329110..23337109hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477198
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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