A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564340



Internal ID16351749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35534869..35536453hg38UCSC Ensembl
Innerchr14:36004075..36005659hg19UCSC Ensembl
Innerchr14:35073826..35075410hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381585
hg191585
hg181585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825764
Samples
Known GenesINSM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564340
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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