A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933730



Internal ID22709045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92771249..92772757hg38UCSC Ensembl
chr15:93314479..93315987hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381509
hg191509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373684
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933730
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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