A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068569



Internal ID21475589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118506121..118506121hg38UCSC Ensembl
chr10:120265633..120265633hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641049
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068569
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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