A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933662



Internal ID22708976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38988173..38988387hg38UCSC Ensembl
chr13:39562310..39562524hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373500
Samples
Known GenesSTOML3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933662
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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