A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444939



Internal ID22502809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79700792..79701545hg38UCSC Ensembl
chr8:80613027..80613780hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909881
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444939
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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