A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365131



Internal ID22590800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116446135..119236441hg38UCSC Ensembl
chr10:118205647..120995953hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg382790307
hg192790307
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974801
Supporting Variants
Samples
Known GenesC10orf82, CACUL1, CASC2, EIF3A, EMX2, EMX2OS, ENO4, FAM204A, FAM45A, FAM45B, GRK5, HSPA12A, KCNK18, KIAA1598, LINC00867, MIR3663, NANOS1, PDZD8, PNLIP, PNLIPRP1, PNLIPRP2, PNLIPRP3, PRDX3, PRLHR, RAB11FIP2, SFXN4, SLC18A2, SNORA19, VAX1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365131
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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