A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382776



Internal ID21040329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18815497..18967663hg38UCSC Ensembl
chr5:18815606..18967772hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38152167
hg19152167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5686n223
Supporting Variantsnssv18129042
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382776
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