A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829248



Internal ID22604183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23325092..23326422hg38UCSC Ensembl
chr1:23651585..23652915hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg381331
hg191331
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464131
Samples
Known GenesHNRNPR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829248
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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