A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579525



Internal ID20952596
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 StatusM
Merged Variantsdgv2596n223
Supporting Variantsnssv18239710
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)nsv6579525
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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