A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238162



Internal ID20805203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77769486..77769983hg38UCSC Ensembl
chr14:78235829..78236326hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585085
Supporting Variants
Samples
Known GenesC14orf178
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238162
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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