A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094199



Internal ID22003432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73795938..73795938hg38UCSC Ensembl
chr14:74262641..74262641hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607747
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094199
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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