A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568920



Internal ID20941991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36437280..36437859hg38UCSC Ensembl
chr6:36405057..36405636hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270712
Samples
Known GenesPXT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568920
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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