A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974801



Internal ID22749736
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 StatusM
Merged Variants
Supporting Variantsnssv17365131
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)nsv5974801
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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