A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356302



Internal ID22581971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29268756..29271674hg38UCSC Ensembl
chr11:29290303..29293221hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg382919
hg192919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911728
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356302
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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