A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570036



Internal ID21518399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172570746..172570821hg38UCSC Ensembl
chr5:171997749..171997824hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133087
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570036
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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