A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072616



Internal ID21501472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93914306..93914306hg38UCSC Ensembl
chr10:95674063..95674063hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642054
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072616
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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