A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481026



Internal ID22538930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11619853..11631189hg38UCSC Ensembl
chrUn_gl000229:8478..19814hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3811337
hg1911337
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481026
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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