A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17581224



Internal ID21773267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54578670..59501927hg38UCSC Ensembl
chr11:54694206..59269400hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg384923258
hg194575195
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6101017
Supporting Variants
Samples
Known GenesAPLNR, BTBD18, C11orf31, CLP1, CNTF, CTNND1, DTX4, FAM111A, FAM111B, GLYAT, GLYATL1, GLYATL2, LOC283194, LPXN, LRRC55, MED19, MIR130A, MIR6128, MPEG1, OR10AG1, OR10Q1, OR10W1, OR1S1, OR1S2, OR4A15, OR4A16, OR4C11, OR4C15, OR4C16, OR4C6, OR4D10, OR4D6, OR4P4, OR4S2, OR5A1, OR5A2, OR5AK2, OR5AK4P, OR5AN1, OR5AP2, OR5AR1, OR5AS1, OR5B12, OR5B17, OR5B2, OR5B21, OR5B3, OR5D13, OR5D14, OR5D16, OR5D18, OR5F1, OR5I1, OR5J2, OR5L1, OR5L2, OR5M1, OR5M10, OR5M11, OR5M3, OR5M8, OR5M9, OR5R1, OR5T1, OR5T2, OR5T3, OR5W2, OR6Q1, OR7E5P, OR8H1, OR8H2, OR8H3, OR8I2, OR8J1, OR8J3, OR8K1, OR8K3, OR8K5, OR8U1, OR8U8, OR9G1, OR9G4, OR9G9, OR9I1, OR9Q1, OR9Q2, P2RX3, PRG2, PRG3, RTN4RL2, SERPING1, SLC43A1, SLC43A3, SMTNL1, SSRP1, TIMM10, TMX2, TMX2-CTNND1, TNKS1BP1, TRIM48, TRIM51, TRIM51HP, UBE2L6, YPEL4, ZDHHC5, ZFP91, ZFP91-CNTF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17581224
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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