A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930966



Internal ID22706242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4627539..4627831hg38UCSC Ensembl
chr16:4677540..4677832hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384077
Samples
Known GenesMGRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930966
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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