A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270044



Internal ID20837084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153683778..158757107hg38UCSC Ensembl
chr6:154004913..159178139hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg385073330
hg195173227
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573838
Supporting Variants
Samples
Known GenesARID1B, CLDN20, CNKSR3, DYNLT1, GTF2H5, IPCEF1, MIR3692, MIR4466, MIR7161, NOX3, OPRM1, SCAF8, SERAC1, SNX9, SYNJ2, SYNJ2-IT1, SYTL3, TFB1M, TIAM2, TMEM181, TMEM242, TULP4, ZDHHC14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270044
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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