A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583395



Internal ID20956466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21535517..21536332hg38UCSC Ensembl
chr18:19115478..19116293hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3325n223
Supporting Variantsnssv18244132
Samples
Known GenesESCO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583395
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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