A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027897



Internal ID21937240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1714130..1726470hg38UCSC Ensembl
chr11:1735360..1747700hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3812341
hg1912341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580545
Samples
Known GenesMOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027897
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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