A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585366



Internal ID21533912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32524480..32542385hg38UCSC Ensembl
chr17:30851498..30869403hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3817906
hg1917906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086108
SamplesHG00096
Known GenesMYO1D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585366
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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