A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239710



Internal ID20806750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77618608..83164280hg38UCSC Ensembl
chr15:77910950..83833032hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg385545673
hg195922083
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579525
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, HDGFRP3, HOMER2, HYKK, IDH3A, IL16, IREB2, KIAA1024, KIAA1199, LINC00927, LINGO1, LOC253044, LOC283692, LOC283693, LOC338963, LOC645752, LOC646938, LOC727751, LOC729911, LOC80154, LOC91450, MESDC1, MESDC2, MEX3B, MIR184, MIR4514, MIR4515, MIR5003, MIR549, MORF4L1, MTHFS, PSMA4, RASGRF1, RPS17, RPS17L, SCARNA15, SH2D7, ST20, ST20-MTHFS, STARD5, TBC1D2B, TM6SF1, TMC3, TMED3, UBE2Q2P2, UBE2Q2P3, WDR61, WHAMM, ZFAND6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239710
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer