A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574060



Internal ID21522472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15592530..15592697hg38UCSC Ensembl
chr3:15634037..15634204hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128426
SamplesHG00512
Known GenesHACL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574060
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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