A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766827



Internal ID18965782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166707104..170282226hg38UCSC Ensembl
chr1:166676341..170251367hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg383575123
hg193575027
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078878
Supporting Variants
SamplesKWP1
Known GenesADCY10, ANKRD36BP1, ATP1B1, BLZF1, C1orf112, CCDC181, CD247, CREG1, DCAF6, DPT, DUSP27, F5, GPA33, GPR161, ILDR2, KIFAP3, LINC00626, LINC00970, LINC01142, LOC100505918, MAEL, METTL11B, METTL18, MIR3119-1, MIR3119-2, MIR557, MPC2, MPZL1, NME7, POGK, POU2F1, RCSD1, SCYL3, SELE, SELL, SELP, SFT2D2, SLC19A2, TADA1, TBX19, TIPRL, XCL1, XCL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766827
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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