A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496449



Internal ID273525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35699850..35707000hg38UCSC Ensembl
chr11:35721398..35728548hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg387151
hg197151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044249
Samples
Known GenesTRIM44
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496449
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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