A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575274



Internal ID21523701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:5811777..5811834hg38UCSC Ensembl
chr4:5813504..5813561hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127452
SamplesNA19239
Known GenesEVC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575274
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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