A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451855



Internal ID22509727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119038671..119041220hg38UCSC Ensembl
chr11:118909381..118911930hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382550
hg192550
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851646
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451855
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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