A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561221



Internal ID20934292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38723671..38724078hg38UCSC Ensembl
chr6:38691447..38691854hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270797
Samples
Known GenesDNAH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561221
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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