A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598770



Internal ID21547398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38665238..38665543hg38UCSC Ensembl
chr11:38686788..38687093hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074908
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598770
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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