A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068331



Internal ID21449697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113263920..113263920hg38UCSC Ensembl
chr10:115023679..115023679hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38997
hg19997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5638448
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068331
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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