A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129909



Internal ID20696949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2712602..2715236hg38UCSC Ensembl
chr5:2712716..2715350hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382635
hg192635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387326
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00134


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