A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508277



Internal ID284972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16768992..16770572hg38UCSC Ensembl
chr11:16790539..16792119hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381581
hg191581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17042999
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508277
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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