A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573838



Internal ID20946909
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 StatusM
Merged Variants
Supporting Variantsnssv18270044
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)nsv6573838
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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