A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410308



Internal ID21067861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60412183..60417571hg38UCSC Ensembl
chr5:59708010..59713398hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg385389
hg195389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133129
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410308
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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