A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589905



Internal ID20962976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52645354..52645853hg38UCSC Ensembl
chr14:53112072..53112571hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230040
Samples
Known GenesERO1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589905
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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