A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467006



Internal ID22524898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60044479..60056509hg38UCSC Ensembl
chr11:59811952..59823982hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3812031
hg1912031
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858743
Supporting Variants
Samples
Known GenesOOSP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467006
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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