A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499663



Internal ID276627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72908459..72914518hg38UCSC Ensembl
chr11:72619504..72625563hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg386060
hg196060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17048285
Samples
Known GenesFCHSD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499663
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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