A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936081



Internal ID22711431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50240330..50240687hg38UCSC Ensembl
chr19:50743587..50743944hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393309
Samples
Known GenesMYH14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936081
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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