A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268529



Internal ID20835569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113354785..113355464hg38UCSC Ensembl
chr6:113675987..113676666hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38680
hg19680
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557905
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268529
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00027


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer