A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535072



Internal ID310784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19400287..19400291hg38UCSC Ensembl
chr11:19421834..19421838hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044721
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535072
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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