A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069765



Internal ID21479717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25822719..25822719hg38UCSC Ensembl
chr10:26111648..26111648hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639669
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069765
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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