A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577377



Internal ID20950448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61659712..61660219hg38UCSC Ensembl
chr18:59326945..59327452hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244719
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577377
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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