A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480262



Internal ID22538165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25549947..25554846hg38UCSC Ensembl
chr21:26922259..26927158hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874814
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480262
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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