A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560587



Internal ID20933658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56332312..57501978hg38UCSC Ensembl
chr6:56197110..57366877hg19UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg381169667
hg191169768
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270969
Samples
Known GenesBAG2, BEND6, DST, KIAA1586, PRIM2, RAB23, RNU6-71P, ZNF451
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560587
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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