A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2793488



Internal ID21238826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52707299..52707410hg38UCSC Ensembl
chr13:53281434..53281545hg19UCSC 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 Variantsnssv13696457
Samples
Known GenesLECT1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2793488
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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