A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147806



Internal ID19195486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93874469..93880102hg38UCSC Ensembl
Outerchr11:93607635..93613268hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385634
hg195634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996590
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147806
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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