A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136037



Internal ID19269050
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 StatusM
Merged Variants
Supporting Variantsnssv3966587, nssv3980276
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136037
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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