A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020567



Internal ID20587607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68391236..68395112hg38UCSC Ensembl
chr14:68857953..68861829hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg383877
hg193877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475738
Supporting Variants
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020567
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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