A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421696



Internal ID200760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161576587..161662587hg38UCSC Ensembl
chr1:161546377..161632377hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3886001
hg1986001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16892417
Samples
Known GenesFCGR2C, FCGR3B, HSPA7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421696
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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