A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394460



Internal ID21052013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8783641..9446671hg38UCSC Ensembl
chr5:8783753..9446783hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38663031
hg19663031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134764
Samples
Known GenesMIR4636, SEMA5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394460
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