A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068571



Internal ID21503368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118685271..118685271hg38UCSC Ensembl
chr10:120444783..120444783hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633895
Supporting Variants
SamplesNA19239
Known GenesCACUL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068571
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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