A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598249



Internal ID20971320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71458202..71459765hg38UCSC Ensembl
chr18:69125438..69127001hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg381564
hg191564
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3405n223
Supporting Variantsnssv18244781
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598249
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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