A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894196



Internal ID22669267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16822911..16823695hg38UCSC Ensembl
chr5:16823020..16823804hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428798
Samples
Known GenesMYO10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894196
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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