A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136138



Internal ID18919769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:90075532..90090132hg38UCSC Ensembl
Outerchr11:89808700..89823300hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3814601
hg1914601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989743
SamplesKWS2
Known GenesUBTFL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136138
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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