A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572537



Internal ID21520928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26390063..26403344hg38UCSC Ensembl
chr3:26431554..26444835hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3813282
hg1913282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138175
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572537
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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