A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565221



Internal ID16005944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:77829108..77832389hg38UCSC Ensembl
Innerchr14:78295451..78298732hg19UCSC Ensembl
Innerchr14:77365204..77368485hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg383282
hg193282
hg183282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3785n54
Supporting Variantsnssv829578
Samples
Known GenesADCK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565221
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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