A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239779



Internal ID20806819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81455708..83007678hg38UCSC Ensembl
chr15:81748049..83676430hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381551971
hg191928382
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581891
Supporting Variants
Samples
Known GenesADAMTS7P1, AP3B2, C15orf40, CPEB1, CSPG4P8, EFTUD1, FAM103A1, FAM154B, FSD2, GOLGA6L10, GOLGA6L20, GOLGA6L9, HOMER2, LOC283692, LOC283693, LOC338963, LOC727751, LOC80154, MEX3B, RPS17, RPS17L, SCARNA15, UBE2Q2P2, UBE2Q2P3, WHAMM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239779
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00026


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