A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518636



Internal ID295016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11547088..11547186hg38UCSC Ensembl
chr19:11657903..11658001hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721421
Samples
Known GenesCNN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518636
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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