A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351382



Internal ID22577051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76712920..76814129hg38UCSC Ensembl
chr10:78472678..78573887hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38101210
hg19101210
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974011
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351382
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