A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467929



Internal ID22525818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126314335..126317274hg38UCSC Ensembl
chr11:126184230..126187169hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382940
hg192940
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859972
Supporting Variants
Samples
Known GenesDCPS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467929
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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