A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570929



Internal ID21519301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183464234..183464299hg38UCSC Ensembl
chr4:184385387..184385452hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126221
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570929
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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