A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468831



Internal ID22526720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70228340..70237594hg38UCSC Ensembl
chr11:70074446..70083700hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg389255
hg199255
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849890
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468831
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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