A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877114



Internal ID22652077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50607432..50609497hg38UCSC Ensembl
chr22:51045860..51047925hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg382066
hg192066
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484295
Samples
Known GenesMAPK8IP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877114
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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