A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593872



Internal ID20966943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22645078..22646270hg38UCSC Ensembl
chr18:20225041..20226233hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381193
hg191193
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3326n223
Supporting Variantsnssv18246123
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593872
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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