A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081871



Internal ID21442722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93731212..93731212hg38UCSC Ensembl
chr14:94197558..94197558hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662504
Supporting Variants
SamplesHG00732
Known GenesPRIMA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081871
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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