A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027096



Internal ID21936439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50554423..50554807hg38UCSC Ensembl
chr13:51128559..51128943hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603316
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027096
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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