A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359219



Internal ID22584888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32994272..32994333hg38UCSC Ensembl
chr10:33283200..33283261hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927110
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359219
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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