A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236667



Internal ID20803707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:107695100..107696032hg38UCSC Ensembl
chr12:108088877..108089809hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38933
hg19933
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592456
Supporting Variants
Samples
Known GenesPWP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236667
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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