A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215057



Internal ID22361508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76431269..76437508hg38UCSC Ensembl
chr11:76142313..76148552hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg386240
hg196240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357951
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215057
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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