A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829394



Internal ID22604329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:231844836..231846161hg38UCSC Ensembl
chr1:231980582..231981907hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg381326
hg191326
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453403
Samples
Known GenesDISC1, TSNAX-DISC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829394
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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