A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567949



Internal ID21516291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43100111..43100195hg38UCSC Ensembl
chr3:43141603..43141687hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132095
SamplesNA19239
Known GenesPOMGNT2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567949
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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