A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580114



Internal ID20953185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31606166..31607086hg38UCSC Ensembl
chr14:32075372..32076292hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38921
hg19921
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2090n223
Supporting Variantsnssv18235456
Samples
Known GenesNUBPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580114
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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