A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595210



Internal ID20968281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:47568608..48389263hg38UCSC Ensembl
chr18:45094979..45915634hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38820656
hg19820656
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246908
Samples
Known GenesSMAD2, ZBTB7C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595210
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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