A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077786



Internal ID19319270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94937462..94939463hg38UCSC Ensembl
chr14:95403799..95405800hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg382002
hg192002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767913
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077786
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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