A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892709



Internal ID22667763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49888156..49888455hg38UCSC Ensembl
chr3:49925589..49925888hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417473
Samples
Known GenesMST1R
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892709
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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