A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482818



Internal ID22540724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27408890..27422972hg38UCSC Ensembl
chr22:27804851..27818933hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3814083
hg1914083
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880156
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482818
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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