A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570019



Internal ID20943090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65276232..66914056hg38UCSC Ensembl
chr6:65986125..67623949hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg381637825
hg191637825
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6218n223
Supporting Variantsnssv18273939
Samples
Known GenesEYS, LOC441155, SLC25A51P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570019
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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