A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581947



Internal ID21530453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15592530..15592613hg38UCSC Ensembl
chr3:15634037..15634120hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125032
SamplesHG00731
Known GenesHACL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581947
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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