A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884100



Internal ID22659082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155593795..155663546hg38UCSC Ensembl
chr1:155563586..155633337hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3869752
hg1969752
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351618
Samples
Known GenesMSTO1, MSTO2P, YY1AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884100
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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