A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18019143



Internal ID20586183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51383871..51386453hg38UCSC Ensembl
chr14:51850589..51853171hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg382583
hg192583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486705
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18019143
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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