A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884379



Internal ID22659361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203918538..203920757hg38UCSC Ensembl
chr1:203887666..203889885hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382220
hg192220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884379
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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