A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482948



Internal ID22540854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38517046..38519683hg38UCSC Ensembl
chr22:38913051..38915688hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg382638
hg192638
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872115
Supporting Variants
Samples
Known GenesDMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482948
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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