A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571534



Internal ID21519914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23434029..23438333hg38UCSC Ensembl
chr3:23475520..23479824hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg384305
hg194305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136043
SamplesHG01114
Known GenesMIR548AC, UBE2E2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571534
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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