A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351342



Internal ID22577011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50024649..50153348hg38UCSC Ensembl
chr10:51784409..51913108hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38128700
hg19128700
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977099
Supporting Variants
Samples
Known GenesFAM21A, FAM21B, FLJ31813
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351342
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