A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565621



Internal ID16006344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94096847..94117658hg38UCSC Ensembl
Innerchr14:94563193..94583995hg19UCSC Ensembl
Innerchr14:93632946..93653748hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3820812
hg1920803
hg1820803
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832700
Samples
Known GenesIFI27, IFI27L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565621
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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