A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998119



Internal ID17291071
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 StatusS
Merged Variantsnsv951277
Supporting Variants
SamplesBILGI_BIOE
Known GenesMIR6744, MUC5B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998119
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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