A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029150



Internal ID21938493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113699239..113699294hg38UCSC Ensembl
chr11:113569961..113570016hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601255
Samples
Known GenesTMPRSS5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029150
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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