A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998149



Internal ID16944415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:9087954..9098353hg38UCSC Ensembl
Outerchr11:9109501..9119900hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3810400
hg1910400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951307
Supporting Variants
SamplesBILGI_BIOE
Known GenesKRT8P41, MIR5691, SCUBE2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998149
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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