A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18018209



Internal ID20585249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39212562..39218569hg38UCSC Ensembl
chr14:39681766..39687773hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg386008
hg196008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487199
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18018209
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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