A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460729



Internal ID22518612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33993752..33996552hg38UCSC Ensembl
chr11:34015299..34018099hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382801
hg192801
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852690
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460729
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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