A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580637



Internal ID21529129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183336717..183336800hg38UCSC Ensembl
chr4:184257870..184257953hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132167
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580637
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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