A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595106



Internal ID20968177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92377901..102079487hg38UCSC Ensembl
chr10:94137658..103839244hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg389701587
hg199701587
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235586
Samples
Known GenesABCC2, ALDH18A1, ANKRD2, ARHGAP19, ARHGAP19-SLIT1, AVPI1, BLNK, BLOC1S2, BTRC, C10orf12, C10orf129, C10orf131, C10orf2, C10orf62, C10orf76, CC2D2B, CCNJ, CEP55, CHUK, CNNM1, COX15, CPN1, CRTAC1, CUTC, CWF19L1, CYP26A1, CYP26C1, CYP2C18, CYP2C19, CYP2C8, CYP2C9, DNMBP, DNMBP-AS1, DNTT, DPCD, ENTPD1, ENTPD1-AS1, ENTPD7, ERLIN1, EXOC6, EXOSC1, FAM178A, FBXW4, FFAR4, FGF8, FRA10AC1, FRAT1, FRAT2, GOLGA7B, GOT1, HELLS, HHEX, HIF1AN, HOGA1, HPS1, HPS6, HPSE2, IDE, KAZALD1, KCNIP2, KCNIP2-AS1, KIF11, LBX1, LBX1-AS1, LCOR, LGI1, LINC00263, LINC00866, LOC100505540, LOXL4, LZTS2, MARK2P9, MARVELD1, MGEA5, MIR1287, MIR3157, MIR3158-1, MIR3158-2, MIR4685, MIR5692C2, MIR608, MMS19, MORN4, MRPL43, MYOF, NDUFB8, NKX2-3, NOC3L, NPM3, OPALIN, PAX2, PDE6C, PDLIM1, PDZD7, PGAM1, PI4K2A, PIK3AP1, PIPSL, PKD2L1, PLCE1, PLCE1-AS1, POLL, PYROXD2, R3HCC1L, RBP4, RRP12, SCD, SEC31B, SEMA4G, SFRP5, SFXN3, SLC25A28, SLC35G1, SLIT1, SNORA12, SORBS1, TBC1D12, TCTN3, TLL2, TLX1, TLX1NB, TM9SF3, UBTD1, WNT8B, ZDHHC16, ZFYVE27, ZNF518A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595106
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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