A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828540



Internal ID22603475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171095828..171102236hg38UCSC Ensembl
chr1:171064969..171071377hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg386409
hg196409
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464669, nssv17466190
Samples
Known GenesFMO3, MIR1295A, MIR1295B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828540
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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