A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239428



Internal ID20806468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28174418..30818114hg38UCSC Ensembl
chr15:28419564..31110317hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg382643697
hg192690754
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577000
Supporting Variants
Samples
Known GenesAPBA2, ARHGAP11B, CHRFAM7A, DKFZP434L187, FAM189A1, GOLGA6L7P, GOLGA8F, GOLGA8G, GOLGA8H, GOLGA8J, GOLGA8M, GOLGA8T, HERC2, HERC2P10, HERC2P9, LOC100288637, LOC100289656, LOC101059918, LOC646278, MIR4509-1, MIR4509-2, MIR4509-3, NDNL2, TJP1, ULK4P1, ULK4P2, ULK4P3, WHAMMP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239428
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00431


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