A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889404



Internal ID22664421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39612492..39617239hg38UCSC Ensembl
chr4:39614112..39618859hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg384748
hg194748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418099
Samples
Known GenesSMIM14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889404
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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