A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592711



Internal ID21541295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36625907..36633260hg38UCSC Ensembl
chr11:36647457..36654810hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg387354
hg197354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074424
SamplesHG03125
Known GenesC11orf74
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592711
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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