A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454405



Internal ID22512281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63256115..63257329hg38UCSC Ensembl
chr11:63023587..63024801hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381215
hg191215
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859540
Supporting Variants
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454405
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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