A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944963



Internal ID22720435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59317963..59389505hg38UCSC Ensembl
chr15:59610162..59681704hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3871543
hg1971543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372288
Samples
Known GenesMYO1E
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944963
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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