A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957369



Internal ID16959556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:17925185..17925265hg38UCSC Ensembl
Outerchr11:17946732..17946812hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005099
SamplesBILGI_BIOE
Known GenesSERGEF
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957369
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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