A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662505



Internal ID21610810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78226793..78226793hg38UCSC Ensembl
chr15:78519135..78519135hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092602, nssv17096123
SamplesHG03125, NA18939
Known GenesACSBG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662505
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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