A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14362974



Internal ID22130502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131865835..131865970hg38UCSC Ensembl
chr11:131735729..131735864hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212844
Supporting Variants
SamplesHG00513
Known GenesNTM
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14362974
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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