A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901879



Internal ID22677032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129976332..129976433hg38UCSC Ensembl
chr3:129695175..129695276hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391460
Samples
Known GenesTRH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901879
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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