A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589645



Internal ID20962716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20450832..20451440hg38UCSC Ensembl
chr14:20918991..20919599hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231747
Samples
Known GenesOSGEP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589645
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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