A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588138



Internal ID20961209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3608158..3608884hg38UCSC Ensembl
chr18:3608156..3608882hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3268n223
Supporting Variantsnssv18244208
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588138
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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