A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499382



Internal ID276356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9582507..9583631hg38UCSC Ensembl
chr11:9604054..9605178hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381125
hg191125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041269
Samples
Known GenesWEE1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499382
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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