A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097291



Internal ID21510250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45914205..45914205hg38UCSC Ensembl
chr17:43991571..43991571hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661178
Supporting Variants
SamplesNA24385
Known GenesMAPT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097291
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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