A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247971



Internal ID20815011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:163441141..169028378hg38UCSC Ensembl
chr1:163410931..168997616hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg385587238
hg195586686
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540250
Supporting Variants
Samples
Known GenesADCY10, ALDH9A1, ANKRD36BP1, CD247, CREG1, DCAF6, DPT, DUSP27, FAM78B, FMO9P, GPA33, GPR161, ILDR2, LINC00626, LINC00970, LMX1A, LOC100505795, LOC100505918, LOC400794, LOC440700, LRRC52, MAEL, MGST3, MIR3658, MIR557, MIR921, MPC2, MPZL1, PBX1, POGK, POU2F1, RCSD1, RXRG, SFT2D2, TADA1, TBX19, TIPRL, TMCO1, UCK2, XCL1, XCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247971
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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