A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564883



Internal ID16352292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:60862272..60907932hg38UCSC Ensembl
Innerchr14:61328990..61374650hg19UCSC Ensembl
Innerchr14:60398743..60444403hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3845661
hg1945661
hg1845661
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv828208
Samples
Known GenesMNAT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564883
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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