A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600390



Internal ID21549030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14326764..14327079hg38UCSC Ensembl
chr11:14348310..14348625hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073392
SamplesHG00731
Known GenesRRAS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600390
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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