A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034382



Internal ID21943725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52707314..52707423hg38UCSC Ensembl
chr13:53281449..53281558hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615125
Samples
Known GenesLECT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034382
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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