A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595922



Internal ID20968993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78354961..78401294hg38UCSC Ensembl
chr18:76114961..76161294hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3846334
hg1946334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244849
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595922
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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