A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574205



Internal ID21522617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41225545..41230222hg38UCSC Ensembl
chr4:41227562..41232239hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg384678
hg194678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138623
SamplesHG03683
Known GenesUCHL1-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574205
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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