A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015932



Internal ID20582972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103623750..103626357hg38UCSC Ensembl
chr14:104090087..104092694hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg382608
hg192608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497709
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015932
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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