A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894639



Internal ID22669713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197775417..197775515hg38UCSC Ensembl
chr3:197502288..197502386hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426910
Samples
Known GenesFYTTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894639
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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