A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454873



Internal ID22512750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97963770..97965769hg38UCSC Ensembl
chr11:97834498..97836497hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856767
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454873
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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