A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186542



Internal ID20753582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67857575..68048882hg38UCSC Ensembl
chr14:68324292..68515599hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38191308
hg19191308
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488156
Supporting Variants
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186542
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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