A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219227



Internal ID20786267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49695913..49696377hg38UCSC Ensembl
chr14:50162631..50163095hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588585
Supporting Variants
Samples
Known GenesKLHDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219227
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