A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662152



Internal ID21610457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78195467..78195467hg38UCSC Ensembl
chr15:78487809..78487809hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088140
SamplesHG03125
Known GenesACSBG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662152
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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