A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564106



Internal ID16004829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26429752..26457905hg38UCSC Ensembl
Innerchr14:26898958..26927111hg19UCSC Ensembl
Innerchr14:25968798..25996951hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3828154
hg1928154
hg1828154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825048
Samples
Known GenesNOVA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564106
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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