A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480989



Internal ID22538893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:10939934..10942990hg38UCSC Ensembl
chrUn_gl000241:15362..18418hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383057
hg193057
Variant TypeOTHER copy number variation
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869189
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480989
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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