A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020572



Internal ID20587612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68523610..68548242hg38UCSC Ensembl
chr14:68990327..69014959hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3824633
hg1924633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475865
Supporting Variants
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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