A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885200



Internal ID22660185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3964396..3966453hg38UCSC Ensembl
chr19:3964394..3966451hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382058
hg192058
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475386
Samples
Known GenesDAPK3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885200
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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