A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901098



Internal ID22676246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51736863..51744675hg38UCSC Ensembl
chr3:51770879..51778691hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg387813
hg197813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422678
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901098
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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