A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574706



Internal ID20947777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25283854..25284571hg38UCSC Ensembl
chr6:25284082..25284799hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270887
Samples
Known GenesLRRC16A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574706
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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