A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953287



Internal ID22728578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27931986..27932288hg38UCSC Ensembl
chr22:28327974..28328276hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403183
Samples
Known GenesTTC28-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953287
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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