A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216477



Internal ID20783517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60411801..60438200hg38UCSC Ensembl
chr5:59707628..59734027hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3826400
hg1926400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6400421
Supporting Variants
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216477
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0012


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