A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398809



Internal ID21056362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:59345150..59393191hg38UCSC Ensembl
chr5:58640976..58689017hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3848042
hg1948042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134342
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398809
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