A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929701



Internal ID22704958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55459711..55460186hg38UCSC Ensembl
chr15:55751909..55752384hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369985
Samples
Known GenesDYX1C1, DYX1C1-CCPG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929701
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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