A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577233



Internal ID20950304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32309780..32314967hg38UCSC Ensembl
chr18:29889743..29894930hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg385188
hg195188
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244073
Samples
Known GenesGAREM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577233
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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