A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842523



Internal ID22617458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181222027..181225926hg38UCSC Ensembl
chr5:180649027..180652926hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495075
Samples
Known GenesMIR4638, TRIM41
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842523
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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