A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999647



Internal ID16945913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:133891206..133952805hg38UCSC Ensembl
Outerchr11:133761101..133822700hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3861600
hg1961600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952765
Supporting Variants
SamplesBILGI_BIOE
Known GenesIGSF9B, MIR4697, MIR4697HG
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999647
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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