A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510762



Internal ID287370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2170798..2178040hg38UCSC Ensembl
chr11:2192028..2199270hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg387243
hg197243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043584
Samples
Known GenesMIR4686, TH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510762
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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