A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928117



Internal ID22703352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95546631..95547142hg38UCSC Ensembl
chr15:96089860..96090371hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373070
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928117
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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