A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088561



Internal ID21441562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25367180..25367180hg38UCSC Ensembl
chr15:25612327..25612327hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656446
Supporting Variants
SamplesHG00732
Known GenesUBE3A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088561
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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