A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125534



Internal ID18901215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:113934810..113935455hg38UCSC Ensembl
Outerchr11:113805532..113806177hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38646
hg19646
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983714
SamplesKWS2
Known GenesHTR3B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125534
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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