A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458005



Internal ID22515886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10942900..10956502hg38UCSC Ensembl
chr11:10964447..10978049hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3813603
hg1913603
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850360
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458005
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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