A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460585



Internal ID22518468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111157803..111162637hg38UCSC Ensembl
chr11:111028527..111033361hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg384835
hg194835
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866600
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460585
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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