A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482868



Internal ID22540774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31605142..31615340hg38UCSC Ensembl
chr22:32001128..32011326hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3810199
hg1910199
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867972
Supporting Variants
Samples
Known GenesSFI1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482868
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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