A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568245



Internal ID20941316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107045215..107053291hg38UCSC Ensembl
chr6:107366419..107374495hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg388077
hg198077
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269786
Samples
Known GenesC6orf203
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568245
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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