A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040420



Internal ID21949763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88745942..88785661hg38UCSC Ensembl
chr11:88479110..88518829hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3839720
hg1939720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595706
Samples
Known GenesGRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040420
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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