A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900171



Internal ID22675311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5113815..5113891hg38UCSC Ensembl
chr3:5155500..5155576hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419299
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900171
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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