A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662231



Internal ID21610536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71999674..71999674hg38UCSC Ensembl
chr14:72466391..72466391hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092736
SamplesHG00731
Known GenesRGS6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662231
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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