A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465775



Internal ID22523664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124037281..124050758hg38UCSC Ensembl
chr11:123907988..123921465hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3813478
hg1913478
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851700
Supporting Variants
Samples
Known GenesOR10G7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465775
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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