A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509874



Internal ID286513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75646849..75648528hg38UCSC Ensembl
chr11:75357894..75359573hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg381680
hg191680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17048487
Samples
Known GenesMAP6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509874
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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