A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662177



Internal ID21610482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26746581..26746581hg38UCSC Ensembl
chr15:26991728..26991728hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093299
SamplesHG00731
Known GenesGABRB3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662177
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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