A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901311



Internal ID22676461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105831839..105831915hg38UCSC Ensembl
chr3:105550683..105550759hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17408650
Samples
Known GenesCBLB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901311
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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