A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564389



Internal ID20937460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42628615..42629089hg38UCSC Ensembl
chr6:42596353..42596827hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271310
Samples
Known GenesUBR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564389
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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