A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147491



Internal ID346672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35697613..35708742hg38UCSC Ensembl
chr11:35719161..35730290hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3811130
hg1911130
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv71n206
Supporting Variantsnssv17044246
Samples
Known GenesTRIM44
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147491
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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