A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933490



Internal ID22708803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52707298..52707409hg38UCSC Ensembl
chr13:53281433..53281544hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379598
Samples
Known GenesLECT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933490
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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