A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907110



Internal ID22682315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139168368..139172877hg38UCSC Ensembl
chr3:138887210..138891719hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg384510
hg194510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398696
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907110
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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