A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583005



Internal ID21531524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158353109..158363138hg38UCSC Ensembl
chr4:159274261..159284290hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3810030
hg1910030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124128
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583005
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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