A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495083



Internal ID272207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85344901..85349943hg38UCSC Ensembl
chr11:85055945..85060987hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg385043
hg195043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049559
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495083
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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