A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561825



Internal ID20934896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21169525..21170610hg38UCSC Ensembl
chr6:21169756..21170841hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381086
hg191086
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6085n223
Supporting Variantsnssv18270192
Samples
Known GenesCDKAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561825
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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