A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406645



Internal ID21064198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:59703301..59705800hg38UCSC Ensembl
chr5:58999127..59001626hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132446
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406645
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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