A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829073



Internal ID22604008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:198832317..198834416hg38UCSC Ensembl
chr1:198801446..198803545hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461620
Samples
Known GenesMIR181A1HG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829073
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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