A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891073



Internal ID22666106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186182198..186184415hg38UCSC Ensembl
chr3:185899987..185902204hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg382218
hg192218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416018
Samples
Known GenesDGKG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891073
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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