A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978819



Internal ID22753754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81455809..83007946hg38UCSC Ensembl
chr15:81748150..83676698hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381552138
hg191928549
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374443
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
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978819
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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