A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092963



Internal ID21483076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91251272..91251272hg38UCSC Ensembl
chr15:91794502..91794502hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651984
Supporting Variants
SamplesHG03732
Known GenesSV2B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092963
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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