A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070402



Internal ID21402403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33867393..33867393hg38UCSC Ensembl
chr10:34156321..34156321hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639556
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070402
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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