A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957228



Internal ID16959415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:117320420..117320616hg38UCSC Ensembl
Outerchr11:117191136..117191332hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002621
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957228
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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