A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403305



Internal ID21060858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87456139..87456597hg38UCSC Ensembl
chr5:86751956..86752414hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403305
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