A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935186



Internal ID22710524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43495064..43495370hg38UCSC Ensembl
chr15:43787262..43787568hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375863
Samples
Known GenesRNU6-28P, TP53BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935186
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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