A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150747



Internal ID19198625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:19701640..19956641hg38UCSC Ensembl
Outerchr14:20169799..20424800hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38255002
hg19255002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996221
SamplesKWB1
Known GenesOR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150747
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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