A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464179



Internal ID22522064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119031712..119034526hg38UCSC Ensembl
chr11:118902422..118905236hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382815
hg192815
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848082
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464179
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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