A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404388



Internal ID21061941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:84694709..84716265hg38UCSC Ensembl
chr5:83990527..84012083hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3821557
hg1921557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135289
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404388
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