A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400472



Internal ID22458342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57521628..57526566hg38UCSC Ensembl
chr19:58032996..58037934hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg384939
hg194939
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971811
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400472
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