A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240489



Internal ID20807529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85570476..90463749hg38UCSC Ensembl
chr15:86113707..91006981hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg384893274
hg194893275
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582041
Supporting Variants
Samples
Known GenesABHD2, ACAN, AEN, AGBL1, AGBL1-AS1, AKAP13, ANPEP, AP3S2, C15orf38, C15orf38-AP3S2, CIB1, DET1, FANCI, GABARAPL3, GDPGP1, HAPLN3, IDH2, IQGAP1, ISG20, KIF7, KLHL25, LINC00052, LINC00925, LINC00928, MESP1, MESP2, MFGE8, MIR1179, MIR1276, MIR3529, MIR5094, MIR6766, MIR7-2, MIR9-3, MRPL46, MRPS11, NGRN, NTRK3, NTRK3-AS1, PEX11A, PLIN1, POLG, RHCG, RLBP1, SEMA4B, TICRR, TTLL13, WDR93, ZNF710, ZNF774
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240489
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00025


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