A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020348



Internal ID20587388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61188971..61194433hg38UCSC Ensembl
chr14:61655689..61661151hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg385463
hg195463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494123
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020348
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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