A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951277



Internal ID17300151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1217871..1262270hg38UCSC Ensembl
Outerchr11:1239101..1283500hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3844400
hg1944400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998119
SamplesBILGI_BIOE
Known GenesMIR6744, MUC5B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951277
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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