A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068338



Internal ID21450624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113435379..113435379hg38UCSC Ensembl
chr10:115195138..115195138hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637501
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068338
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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