A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890436



Internal ID22665464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99605795..99611786hg38UCSC Ensembl
chr3:99324639..99330630hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg385992
hg195992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416933
Samples
Known GenesMIR548G
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890436
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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