A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907378



Internal ID22682586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86573590..86574921hg38UCSC Ensembl
chr3:86622740..86624071hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg381332
hg191332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418509
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907378
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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