A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261231



Internal ID20470449
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 StatusS
Merged Variantsnsv4766814
Supporting Variants
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)nssv16261231
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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