A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098522



Internal ID22007755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52674205..52674205hg38UCSC Ensembl
chr15:52966402..52966402hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604128
Samples
Known GenesFAM214A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098522
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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