A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091616



Internal ID21453856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74259416..74259416hg38UCSC Ensembl
chr14:74726119..74726119hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661444
Supporting Variants
SamplesHG02011
Known GenesVSX2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091616
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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