A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467014



Internal ID22524906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134012485..134014584hg38UCSC Ensembl
chr11:133882380..133884479hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865211
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467014
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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