A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895627



Internal ID22670712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23422802..23422903hg38UCSC Ensembl
chr3:23464293..23464394hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418090
Samples
Known GenesMIR548AC, UBE2E2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895627
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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