A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983714



Internal ID18891961
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 StatusS
Merged Variantsnsv1125534
Supporting Variants
SamplesKWS2
Known GenesHTR3B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983714
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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