A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4009711



Internal ID22071342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101034032..101059664hg38UCSC Ensembl
Outerchr14:101027348..101063077hg38UCSC Ensembl
Innerchr14:101500369..101526001hg19UCSC Ensembl
Outerchr14:101493685..101529414hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3835730
hg1935730
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155041
Supporting Variants
Samples
Known GenesMIR1185-1, MIR1185-2, MIR1193, MIR134, MIR154, MIR300, MIR323B, MIR376A1, MIR376A2, MIR376B, MIR376C, MIR377, MIR381, MIR381HG, MIR382, MIR485, MIR487A, MIR487B, MIR494, MIR495, MIR496, MIR539, MIR543, MIR654, MIR655, MIR668, MIR889
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4009711
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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