A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592169



Internal ID20965240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49610602..49611455hg38UCSC Ensembl
chr14:50077320..50078173hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38854
hg19854
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225541
Samples
Known GenesLRR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592169
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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