A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935368



Internal ID22710708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94777441..94777606hg38UCSC Ensembl
chr15:95320670..95320835hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376727
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935368
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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