A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129168



Internal ID20696208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:25048631..25049083hg38UCSC Ensembl
chr5:25048740..25049192hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387274
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00113


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