A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388806



Internal ID21046359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17400838..17409340hg38UCSC Ensembl
chr5:17400947..17409449hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg388503
hg198503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128497
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388806
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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