A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583014



Internal ID20956085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9037077..9037632hg38UCSC Ensembl
chr18:9037075..9037630hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3277n223
Supporting Variantsnssv18244934
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583014
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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