A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223060



Internal ID22366941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62568201..62568361hg38UCSC Ensembl
chr11:62335673..62335833hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14359771, nssv14359770, nssv14359769, nssv14359768
SamplesHG00512, NA19239, HG00731, HG00732
Known GenesEEF1G
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223060
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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