A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585055



Internal ID20958126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79754380..87461415hg38UCSC Ensembl
chr10:81514136..89221172hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg387707036
hg197707037
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231492
Samples
Known GenesADIRF, AGAP11, ANXA11, BMPR1A, C10orf99, CCSER2, CDHR1, DYDC1, DYDC2, FAM213A, FAM25A, FAM35A, GHITM, GLUD1, GRID1, GRID1-AS1, LDB3, LINC00857, LINC00858, LINC00864, LOC100288974, LOC439994, LOC642361, LRIT1, LRIT2, MAT1A, MBL1P, MIR346, MMRN2, NRG3, NUTM2A, NUTM2A-AS1, NUTM2D, OPN4, PLAC9, RGR, SFTPD, SH2D4B, SNCG, TMEM254, TMEM254-AS1, TSPAN14, WAPAL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585055
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