A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141879



Internal ID18938040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:79656776..87327232hg38UCSC Ensembl
Outerchr10:81416532..89086989hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg387670457
hg197670458
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993386
SamplesKWS2
Known GenesADIRF, AGAP11, ANXA11, BEND3P3, BMPR1A, C10orf99, CCSER2, CDHR1, DYDC1, DYDC2, FAM213A, FAM25A, FAM35A, GHITM, GLUD1, GRID1, GRID1-AS1, LDB3, LINC00857, LINC00858, LOC100288974, LOC642361, LRIT1, LRIT2, MAT1A, MBL1P, MIR346, MMRN2, NRG3, NUTM2A, NUTM2A-AS1, NUTM2B, OPN4, PLAC9, RGR, SFTPD, SH2D4B, SNCG, TMEM254, TMEM254-AS1, TSPAN14, WAPAL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141879
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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