A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509086



Internal ID285753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26684610..26687761hg38UCSC Ensembl
chr11:26706157..26709308hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg383152
hg193152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17042671
Samples
Known GenesSLC5A12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509086
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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