A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951284



Internal ID16953471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:2083671..2218670hg38UCSC Ensembl
Outerchr11:2104901..2239900hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38135000
hg19135000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998126
SamplesBILGI_BIOE
Known GenesIGF2, IGF2-AS, INS, INS-IGF2, MIR4686, MIR483, TH
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951284
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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