A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868108



Internal ID22643043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84829011..84829110hg38UCSC Ensembl
chr1:85294694..85294793hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386574
Samples
Known GenesLPAR3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868108
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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