A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505098



Internal ID22563042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20672939..20674838hg38UCSC Ensembl
chr8:20530450..20532349hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863426
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505098
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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