A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558718



Internal ID20931789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154168717..154169272hg38UCSC Ensembl
chr6:154489852..154490406hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38556
hg19555
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270046
Samples
Known GenesIPCEF1, OPRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558718
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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