A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037240



Internal ID21946583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14326764..14327080hg38UCSC Ensembl
chr11:14348310..14348626hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583609
Samples
Known GenesRRAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037240
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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