A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505140



Internal ID22563084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23276614..23277963hg38UCSC Ensembl
chr8:23134127..23135476hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg381350
hg191350
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867047
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505140
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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