A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590355



Internal ID21538924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43137180..43137424hg38UCSC Ensembl
chr11:43158730..43158974hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074255
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590355
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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