A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766814



Internal ID20542674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153431005..160785696hg38UCSC Ensembl
chr6:153752140..161206728hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg387354692
hg197454589
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261231
Samples
Known GenesACAT2, AIRN, ARID1B, C6orf99, CLDN20, CNKSR3, DYNLT1, EZR, EZR-AS1, FNDC1, GTF2H5, IGF2R, IPCEF1, LOC100129518, LOC729603, LPA, LPAL2, MAS1, MIR3692, MIR3918, MIR4466, MIR7161, MRPL18, NOX3, OPRM1, OSTCP1, PLG, PNLDC1, RSPH3, SCAF8, SERAC1, SLC22A1, SLC22A2, SLC22A3, SNORA20, SNORA29, SNX9, SOD2, SYNJ2, SYNJ2-IT1, SYTL3, TAGAP, TCP1, TFB1M, TIAM2, TMEM181, TMEM242, TULP4, WTAP, ZDHHC14
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766814
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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