A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5503308



Internal ID280142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85057834..85066770hg38UCSC Ensembl
chr11:84768878..84777814hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg388937
hg198937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17059119
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5503308
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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