A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936425



Internal ID22711779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83546127..83546433hg38UCSC Ensembl
chr15:84214879..84215185hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381833
Samples
Known GenesSH3GL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936425
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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