A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18018079



Internal ID20585119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37853937..37858500hg38UCSC Ensembl
chr14:38323142..38327705hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg384564
hg194564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495491
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18018079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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