A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564061



Internal ID16004784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24441932..24476125hg38UCSC Ensembl
Innerchr14:24911138..24945331hg19UCSC Ensembl
Innerchr14:23980978..24015171hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3834194
hg1934194
hg1834194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv824391
Samples
Known GenesSDR39U1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564061
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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