A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593426



Internal ID21542013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67246628..67246693hg38UCSC Ensembl
chr15:67538966..67539031hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095663
SamplesHG00731
Known GenesAAGAB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593426
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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