A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362667



Internal ID22588336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46108417..47381921hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381273505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910146
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362667
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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