A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14360597



Internal ID22251021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68372261..68372391hg38UCSC Ensembl
chr11:68139729..68139859hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229139
Supporting Variants
SamplesHG00733
Known GenesLRP5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14360597
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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