A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583659



Internal ID21532187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153724962..153725042hg38UCSC Ensembl
chr4:154646114..154646194hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130759
SamplesHG00732
Known GenesRNF175
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583659
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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