A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566907



Internal ID21515238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55559798..55560123hg38UCSC Ensembl
chr5:54855626..54855951hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155619
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566907
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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