A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842153



Internal ID22617088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16293635..16300379hg38UCSC Ensembl
chr5:16293744..16300488hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg386745
hg196745
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497023
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842153
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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