A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900779



Internal ID22675925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46616690..46618891hg38UCSC Ensembl
chr3:46658180..46660381hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382202
hg192202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415380
Samples
Known GenesLOC100132146
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900779
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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