A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582806



Internal ID21531322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24501488..24502613hg38UCSC Ensembl
chr4:24503111..24504236hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381126
hg191126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127831
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582806
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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