A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999627



Internal ID16945893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:118892392..118923091hg38UCSC Ensembl
Outerchr11:118763101..118793800hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3830700
hg1930700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952743
Supporting Variants
SamplesBILGI_BIOE
Known GenesBCL9L, CXCR5, MIR4492
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999627
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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