A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565233



Internal ID16352642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:77900624..77924537hg38UCSC Ensembl
Innerchr14:78366967..78390880hg19UCSC Ensembl
Innerchr14:77436720..77460633hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3823914
hg1923914
hg1823914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv829608
Samples
Known GenesADCK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565233
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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