A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564933



Internal ID16005656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:65200828..65243862hg38UCSC Ensembl
Innerchr14:65667546..65710580hg19UCSC Ensembl
Innerchr14:64737299..64780333hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3843035
hg1943035
hg1843035
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv828531
Samples
Known GenesLOC100128233
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564933
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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