A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410280



Internal ID22468150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20320746..20320818hg38UCSC Ensembl
chr6:20320977..20321049hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905154
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410280
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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