A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238394



Internal ID20805434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96457077..96458760hg38UCSC Ensembl
chr14:96923414..96925097hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381684
hg191684
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582082
Supporting Variants
Samples
Known GenesAK7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238394
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