A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17349789



Internal ID22575529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47399270..47399580hg38UCSC Ensembl
chr11:47420821..47421131hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918536
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17349789
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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