A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980276



Internal ID19208466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93057983..93067427hg38UCSC Ensembl
Outerchr11:92791149..92800593hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg389445
hg199445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136037
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980276
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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