A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895453



Internal ID22670535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50589624..50589758hg38UCSC Ensembl
chr3:50627055..50627189hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416506
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895453
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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