A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455776



Internal ID22513653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2112218..2113821hg38UCSC Ensembl
chr11:2133448..2135051hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381604
hg191604
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866530
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455776
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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