A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569026



Internal ID20942097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18212158..18213305hg38UCSC Ensembl
chr6:18212389..18213536hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381148
hg191148
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270644
Samples
Known GenesKDM1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569026
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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