A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854231



Internal ID22629166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62622046..62628633hg38UCSC Ensembl
chr15:62914245..62920832hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg386588
hg196588
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473517
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854231
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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