A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959043



Internal ID19216615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:19684741..19956441hg38UCSC Ensembl
Outerchr14:20152900..20424600hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38271701
hg19271701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118534
Supporting Variants
SamplesKWS1
Known GenesOR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959043
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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