A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929581



Internal ID22704837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8522105..8523121hg38UCSC Ensembl
chr19:8586989..8588005hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393094
Samples
Known GenesMYO1F
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929581
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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