A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108932



Internal ID22018165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33574222..38571003hg38UCSC Ensembl
chr9:33574220..38571000hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg384996782
hg194996781
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585686
Samples
Known GenesALDH1B1, 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
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108932
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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