A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564194



Internal ID16004917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34516439..34560190hg38UCSC Ensembl
Innerchr14:34985645..35029396hg19UCSC Ensembl
Innerchr14:34055396..34099147hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3843752
hg1943752
hg1843752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825155
Samples
Known GenesEAPP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564194
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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