A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097859



Internal ID22007092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91521455..91521455hg38UCSC Ensembl
chr14:91987799..91987799hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614317
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097859
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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