A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239711



Internal ID20806751
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 StatusS
Merged Variantsnsv6578911
Supporting Variants
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)nssv18239711
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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