A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564648



Internal ID20937719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93486731..94421403hg38UCSC Ensembl
chr6:94196449..95131121hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38934673
hg19934673
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272163
Samples
Known GenesTSG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564648
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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