A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367514



Internal ID22593183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44890747..44891219hg38UCSC Ensembl
chr11:44912298..44912770hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914106
Supporting Variants
Samples
Known GenesTSPAN18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367514
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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