A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565885



Internal ID16353294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101700166..101751623hg38UCSC Ensembl
Innerchr14:102166503..102217960hg19UCSC Ensembl
Innerchr14:101236256..101287713hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3851458
hg1951458
hg1851458
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833730
Samples
Known GenesLINC00239
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565885
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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