A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939047



Internal ID22714435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39396176..39396759hg38UCSC Ensembl
chr19:39886816..39887399hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405160
Samples
Known GenesMED29
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939047
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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