A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565169



Internal ID16352578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73561413..73579779hg38UCSC Ensembl
Innerchr14:74028117..74046483hg19UCSC Ensembl
Innerchr14:73097870..73116236hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3818367
hg1918367
hg1818367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3774n54
Supporting Variantsnssv829493
Samples
Known GenesACOT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565169
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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