A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407066



Internal ID21064619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60303394..60341894hg38UCSC Ensembl
chr5:59599221..59637721hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3838501
hg1938501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133122
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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