A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045606



Internal ID98169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32588734..32589011hg38UCSC Ensembl
chr11:32610280..32610557hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498048
Supporting Variants
Samples
Known GenesEIF3M
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045606
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002654


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