A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489789



Internal ID21147342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68144968..68182590hg38UCSC Ensembl
chr14:68611685..68649307hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3837623
hg1937623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020552
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489789
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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