A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450757



Internal ID22508630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62284698..62289183hg38UCSC Ensembl
chr11:62052170..62056655hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg384486
hg194486
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857204
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450757
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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