A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356066



Internal ID21013619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14724004..14726260hg38UCSC Ensembl
chr4:14725628..14727884hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382257
hg192257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18109568
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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