A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495696



Internal ID272796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133926555..133926624hg38UCSC Ensembl
chr11:133796450..133796519hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17051756
Samples
Known GenesIGSF9B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495696
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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