A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587688



Internal ID21536246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26300925..26301167hg38UCSC Ensembl
chr11:26322472..26322714hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073939
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587688
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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