A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16905521



Internal ID4488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84845282..84845990hg38UCSC Ensembl
chr1:85310965..85311673hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38709
hg19709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430058
Supporting Variants
Samples
Known GenesLPAR3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16905521
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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