A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575654



Internal ID20948725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45357323..45358737hg38UCSC Ensembl
chr18:42937288..42938702hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg381415
hg191415
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246863
Samples
Known GenesSLC14A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575654
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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