A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241967



Internal ID20809007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75332404..77948110hg38UCSC Ensembl
chr15:75624745..78240452hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg382615707
hg192615708
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578620
Supporting Variants
Samples
Known GenesC15orf27, COMMD4, CSPG4, DNM1P35, ETFA, FBXO22, FBXO22-AS1, HMG20A, IMP3, ISL2, LINC00597, LINGO1, LOC253044, LOC645752, MAN2C1, MIR4313, MIR631, NEIL1, NRG4, ODF3L1, PEAK1, PSTPIP1, PTPN9, RCN2, SCAPER, SIN3A, SNUPN, SNX33, TSPAN3, TYRO3P, UBE2Q2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241967
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.46825


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