A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066735



Internal ID21434777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123904876..123904876hg38UCSC Ensembl
chr10:125664392..125664392hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5627252
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066735
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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