A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5494592



Internal ID271729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81719358..81977491hg38UCSC Ensembl
chr11:81430400..81688533hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38258134
hg19258134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv84n206
Supporting Variantsnssv17048800
Samples
Known GenesMIR4300
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5494592
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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