A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579202



Internal ID20952273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22805820..22807210hg38UCSC Ensembl
chr14:23275029..23276419hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381391
hg191391
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223504
Samples
Known GenesSLC7A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579202
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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