A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875996



Internal ID22650956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98187604..98189078hg38UCSC Ensembl
chr15:98730833..98732307hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381475
hg191475
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475013
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875996
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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