A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480930



Internal ID22538834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45585062..45589361hg38UCSC Ensembl
chr21:47004976..47009275hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886387
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480930
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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