A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071573



Internal ID21480907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93702516..93702516hg38UCSC Ensembl
chr10:95462273..95462273hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625407
Supporting Variants
SamplesHG03683
Known GenesFRA10AC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071573
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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