A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564333



Internal ID16351742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35534103..35536453hg38UCSC Ensembl
Innerchr14:36003309..36005659hg19UCSC Ensembl
Innerchr14:35073060..35075410hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg382351
hg192351
hg182351
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825752
Samples
Known GenesINSM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564333
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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