A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507287



Internal ID284013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89713648..89886248hg38UCSC Ensembl
chr11:89446816..89619416hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38172601
hg19172601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17050787
Samples
Known GenesMIR5692A1, TRIM49, TRIM53AP, TRIM64B, TRIM77
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507287
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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