A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575810



Internal ID21524242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:29578791..29579112hg38UCSC Ensembl
chr3:29620282..29620603hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137356
SamplesHG00512
Known GenesRBMS3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575810
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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