A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946052



Internal ID22721536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93106544..93111363hg38UCSC Ensembl
chr15:93649773..93654592hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg384820
hg194820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946052
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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