A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568421



Internal ID21516769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:29494832..29495102hg38UCSC Ensembl
chr3:29536323..29536593hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127555
SamplesNA19983
Known GenesRBMS3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568421
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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