A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027797



Internal ID21937140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22316525..22316580hg38UCSC Ensembl
chr11:22338071..22338126hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580636
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027797
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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