A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560363



Internal ID20933434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33533993..38610852hg38UCSC Ensembl
chr9:33533991..38610849hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg385076860
hg195076859
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280515
Samples
Known GenesALDH1B1, ANKRD18A, ANKRD18B, ANXA2P2, ARHGEF39, ARID3C, ATP8B5P, C9orf131, C9orf24, CA9, CCDC107, CCIN, CCL19, CCL21, CCL27, CD72, CLTA, CNTFR, CNTFR-AS1, CREB3, DCAF10, DCAF12, DCTN3, DNAI1, DNAJB5, ENHO, EXOSC3, FAM166B, FAM205A, FAM205B, FAM214B, FAM219A, FAM221B, FAM95C, FANCG, FBXO10, FRMPD1, GALT, GBA2, GLIPR2, GNE, GRHPR, HINT2, HRCT1, IGFBPL1, IL11RA, KIAA1045, KIAA1161, KIF24, LINC00950, LINC00961, LOC100506710, LOC101926900, LOC101929688, MELK, MIR4475, MIR4476, MIR4540, MIR4667, MIR6852, MIR6853, MSMP, NPR2, NUDT2, OR13J1, OR2S2, PAX5, PIGO, POLR1E, PRSS3, PTENP1, PTENP1-AS, RECK, RGP1, RMRP, RNF38, RPP25L, RUSC2, SHB, SIGMAR1, SIT1, SLC25A51, SNORD121A, SNORD121B, SPAG8, STOML2, TESK1, TLN1, TMEM8B, TOMM5, TPM2, TRMT10B, UBAP1, UBAP2, UBE2R2, UNC13B, VCP, ZBTB5, ZCCHC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560363
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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