A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077784



Internal ID19322317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19723940..19956441hg38UCSC Ensembl
chr14:20192099..20424600hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38232502
hg19232502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769673
SamplesKWP1
Known GenesOR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077784
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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