A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830507



Internal ID22605442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84867796..84909748hg38UCSC Ensembl
chr1:85333479..85375431hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3841953
hg1941953
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481816
Samples
Known GenesLPAR3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830507
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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