A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878802



Internal ID22653768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171090573..171102799hg38UCSC Ensembl
chr1:171059714..171071940hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg3812227
hg1912227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360605
Samples
Known GenesFMO3, MIR1295A, MIR1295B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878802
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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