A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566614



Internal ID21514942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43516378..43516446hg38UCSC Ensembl
chr5:43516480..43516548hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132315
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566614
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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