A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578911



Internal ID20951982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77618608..84708062hg38UCSC Ensembl
chr15:77910950..85251293hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg387089455
hg197340344
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2596n223
Supporting Variantsnssv18239711
Samples
Known GenesABHD17C, ACSBG1, ADAMTS7, ADAMTS7P1, ADAMTSL3, ANKRD34C, AP3B2, ARNT2, BCL2A1, BNC1, BTBD1, C15orf26, C15orf37, C15orf40, CHRNA3, CHRNA5, CHRNB4, CIB2, CPEB1, CRABP1, CSPG4P8, CTSH, DNAJA4, DNM1P41, EFTUD1, EFTUD1P1, FAH, FAM103A1, FAM154B, FSD2, GOLGA6L10, GOLGA6L20, GOLGA6L4, GOLGA6L5P, GOLGA6L9, HDGFRP3, HOMER2, HYKK, IDH3A, IL16, IREB2, KIAA1024, KIAA1199, LINC00927, LINC00933, LINGO1, LOC100505679, LOC253044, LOC283692, LOC283693, LOC338963, LOC388152, LOC440300, LOC642423, LOC645752, LOC646938, LOC727751, LOC729911, LOC80154, LOC91450, MESDC1, MESDC2, MEX3B, MIR184, MIR4514, MIR4515, MIR5003, MIR549, MORF4L1, MTHFS, NMB, PSMA4, RASGRF1, RPS17, RPS17L, SCAND2P, SCARNA15, SEC11A, SH2D7, SH3GL3, ST20, ST20-MTHFS, STARD5, TBC1D2B, TM6SF1, TMC3, TMED3, UBE2Q2P1, UBE2Q2P2, UBE2Q2P3, WDR61, WDR73, WHAMM, ZFAND6, ZSCAN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578911
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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