A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489171



Internal ID21146724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57994225..57998008hg38UCSC Ensembl
chr14:58460943..58464726hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg383784
hg193784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019866
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489171
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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