A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931332



Internal ID22706615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57477116..57491787hg38UCSC Ensembl
chr19:57988484..58003155hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3814672
hg1914672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401505
Samples
Known GenesZNF419, ZNF772
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931332
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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