A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14359768



Internal ID22129195
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223060
Supporting Variants
SamplesHG00512
Known GenesEEF1G
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14359768
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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