A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603839



Internal ID21552505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2124044..2125686hg38UCSC Ensembl
chr11:2145274..2146916hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381643
hg191643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074102
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603839
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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