A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600156



Internal ID21548794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68087916..68087965hg38UCSC Ensembl
chr14:68554633..68554682hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091956
SamplesHG00732
Known GenesRAD51B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600156
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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