A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854023



Internal ID22628958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49648475..49658561hg38UCSC Ensembl
chr13:50222611..50232697hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3810087
hg1910087
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv527n209
Supporting Variantsnssv17456054, nssv17457993
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854023
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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