A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288767



Internal ID20497985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52707323..52707435hg38UCSC Ensembl
chr13:53281458..53281570hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740672
Supporting Variants
Samples
Known GenesLECT1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288767
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer