A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829203



Internal ID22604138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220115300..220120336hg38UCSC Ensembl
chr1:220288642..220293678hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg385037
hg195037
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463849
Samples
Known GenesIARS2, MIR194-1, MIR215, RNU5F-1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829203
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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