A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590894



Internal ID20963965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:370228..2243859hg38UCSC Ensembl
chr18:370228..2243859hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg381873632
hg191873632
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3261n223
Supporting Variantsnssv18244229
Samples
Known GenesADCYAP1, C18orf56, CETN1, CLUL1, COLEC12, ENOSF1, LINC00470, TYMS, YES1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590894
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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