A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577464



Internal ID20950535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3416712..3417408hg38UCSC Ensembl
chr18:3416710..3417406hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244174
Samples
Known GenesTGIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577464
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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