A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239708



Internal ID20806748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77618605..83035894hg38UCSC Ensembl
chr15:77910947..83704646hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg385417290
hg195793700
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579530
Supporting Variants
Samples
Known GenesABHD17C, ACSBG1, ADAMTS7, ADAMTS7P1, ANKRD34C, AP3B2, ARNT2, BCL2A1, BTBD1, C15orf26, C15orf37, C15orf40, CHRNA3, CHRNA5, CHRNB4, CIB2, CPEB1, CRABP1, CSPG4P8, CTSH, DNAJA4, EFTUD1, FAH, FAM103A1, FAM154B, FSD2, GOLGA6L10, GOLGA6L20, GOLGA6L9, HOMER2, HYKK, IDH3A, IL16, IREB2, KIAA1024, KIAA1199, LINC00927, LINGO1, LOC253044, LOC283692, LOC283693, LOC338963, LOC645752, LOC646938, LOC727751, LOC729911, LOC80154, LOC91450, MESDC1, MESDC2, MEX3B, MIR184, MIR4514, MIR5003, MIR549, MORF4L1, MTHFS, PSMA4, RASGRF1, RPS17, RPS17L, SCARNA15, SH2D7, ST20, ST20-MTHFS, STARD5, TBC1D2B, TMC3, TMED3, UBE2Q2P2, UBE2Q2P3, WDR61, WHAMM, ZFAND6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239708
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00024


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