A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591090



Internal ID21539662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126974475..126974534hg38UCSC Ensembl
chr11:126844371..126844430hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073091
SamplesHG00731
Known GenesKIRREL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591090
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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