A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073160



Internal ID21448225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134220430..134220430hg38UCSC Ensembl
chr11:134090324..134090324hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661153
Supporting Variants
SamplesHG00733
Known GenesNCAPD3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073160
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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