A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17484305



Internal ID22542213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50644720..50647019hg38UCSC Ensembl
chr22:51083148..51085447hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887116
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17484305
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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