A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116672



Internal ID19267265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:33653938..33654261hg38UCSC Ensembl
Outerchr11:33675484..33675807hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3979236
SamplesKWS2
Known GenesKIAA1549L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116672
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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