A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568396



Internal ID21516743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168440437..168442113hg38UCSC Ensembl
chr4:169361588..169363264hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg381677
hg191677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127018
SamplesNA19983
Known GenesDDX60L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568396
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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