A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559211



Internal ID20932282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93309110..93310391hg38UCSC Ensembl
chr6:94018828..94020109hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381282
hg191282
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272160
Samples
Known GenesEPHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559211
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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