A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564107



Internal ID16004830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26429752..26489004hg38UCSC Ensembl
Innerchr14:26898958..26958210hg19UCSC Ensembl
Innerchr14:25968798..26028050hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3859253
hg1959253
hg1859253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825050, nssv825049
Samples
Known GenesNOVA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564107
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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