A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510981



Internal ID287586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96068235..96069356hg38UCSC Ensembl
chr11:95801399..95802520hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381122
hg191122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049296
Samples
Known GenesMAML2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510981
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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