A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564880



Internal ID16005603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:60397865..60916029hg38UCSC Ensembl
Innerchr14:60864583..61382747hg19UCSC Ensembl
Innerchr14:59934336..60452500hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38518165
hg19518165
hg18518165
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv828205
Samples
Known GenesC14orf39, MNAT1, SIX1, SIX4, SIX6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564880
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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