A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567295



Internal ID20940366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89002520..89003973hg38UCSC Ensembl
chr6:89712239..89713692hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381454
hg191454
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274905
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567295
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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