A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900758



Internal ID22675903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58163939..58164770hg38UCSC Ensembl
chr3:58149666..58150497hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38832
hg19832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424232
Samples
Known GenesFLNB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900758
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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