A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13702117



Internal ID21198403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187413757..187428815hg38UCSC Ensembl
chr3:187131545..187146603hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3815059
hg1915059
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2808914
Supporting Variants
SamplesCHM1
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13702117
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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