A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356469



Internal ID22582138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78291465..78292879hg38UCSC Ensembl
chr10:80051222..80052636hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381415
hg191415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909230
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356469
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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