A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558579



Internal ID20931650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87688180..87688721hg38UCSC Ensembl
chr6:88397898..88398439hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38542
hg19542
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274875
Samples
Known GenesAKIRIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558579
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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