A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17483608



Internal ID22541515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42706809..42708466hg38UCSC Ensembl
chr22:43102815..43104472hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg381658
hg191658
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874699
Supporting Variants
Samples
Known GenesA4GALT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17483608
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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