A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067546



Internal ID21404322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116394458..116394458hg38UCSC Ensembl
chr10:118153970..118153970hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632141
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067546
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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