A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993386



Internal ID18893286
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 StatusS
Merged Variantsnsv1141879
Supporting Variants
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)nssv3993386
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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