A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272733



Internal ID20481951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175231391..175232798hg38UCSC Ensembl
chr1:175200527..175201934hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg381408
hg191408
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4768001
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272733
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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