A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482828



Internal ID22540734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28641411..28645086hg38UCSC Ensembl
chr22:29037399..29041074hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg383676
hg193676
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881030
Supporting Variants
Samples
Known GenesTTC28
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482828
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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