A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357861



Internal ID22306005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73462807..73463071hg38UCSC Ensembl
chr11:73173852..73174116hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218193
Supporting Variants
SamplesNA19240
Known GenesFAM168A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357861
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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