A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905567



Internal ID22680755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184388237..184388392hg38UCSC Ensembl
chr3:184106025..184106180hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421090
Samples
Known GenesCHRD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905567
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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