A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976739



Internal ID19228068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:19714441..19955441hg38UCSC Ensembl
Outerchr14:20182600..20423600hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38241001
hg19241001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124684
Supporting Variants
SamplesKWS2
Known GenesOR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976739
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer