A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568323



Internal ID20941394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84194286..84194550hg38UCSC Ensembl
chr6:84904004..84904268hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274801
Samples
Known GenesKIAA1009
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568323
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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