A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044247



Internal ID97235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35699146..35707563hg38UCSC Ensembl
chr11:35720694..35729111hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg388418
hg198418
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147230
Supporting Variants
Samples
Known GenesTRIM44
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044247
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.061193


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