A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596624



Internal ID21545233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63547722..63547771hg38UCSC Ensembl
chr15:63839921..63839970hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083029
SamplesHG00731
Known GenesUSP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596624
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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