A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403570



Internal ID21061123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:59003667..59004004hg38UCSC Ensembl
chr5:58299494..58299831hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133709
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403570
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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