A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892139



Internal ID22667184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113046781..113046860hg38UCSC Ensembl
chr3:112765628..112765707hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390524
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892139
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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