A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854439



Internal ID22629374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62343343..62345110hg38UCSC Ensembl
chr15:62635542..62637309hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381768
hg191768
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471746
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854439
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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