A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881030



Internal ID22656002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28641411..28645086hg38UCSC Ensembl
chr22:29037399..29041074hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg383676
hg193676
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482828
Samples
Known GenesTTC28
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881030
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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