A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221229



Internal ID22365684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:763165..764482hg38UCSC Ensembl
chr11:763165..764482hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381318
hg191318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14356435
SamplesHG00731
Known GenesTALDO1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221229
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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