A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17484861



Internal ID22542771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50739518..50747099hg38UCSC Ensembl
chr22:51177946..51185527hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg387582
hg197582
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878487
Supporting Variants
Samples
Known GenesACR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17484861
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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