A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608803



Internal ID21800850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53849801..53851324hg38UCSC Ensembl
chr13:54423936..54425459hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381524
hg191524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029307
Supporting Variants
Samples
Known GenesLINC00558
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608803
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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