A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879873



Internal ID22654843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93846643..93846993hg38UCSC Ensembl
chr1:94312199..94312549hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402175
Samples
Known GenesBCAR3, MIR760
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879873
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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