A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124684



Internal ID19279074
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 StatusM
Merged Variantsdgv1050n106
Supporting Variantsnssv3976739
SamplesKWS2
Known GenesOR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124684
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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