A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500705



Internal ID277632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27994706..27994804hg38UCSC Ensembl
chr11:28016253..28016351hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044500
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500705
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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