A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18018749



Internal ID20585789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45276451..45365791hg38UCSC Ensembl
chr14:45745654..45834994hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3889341
hg1989341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18018749
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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