A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879106



Internal ID22654074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57133975..57139167hg38UCSC Ensembl
chr19:57645343..57650535hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg385193
hg195193
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478775
Samples
Known GenesZIM3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879106
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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