A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566069



Internal ID16006792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104719329..104808201hg38UCSC Ensembl
Innerchr14:105185666..105274538hg19UCSC Ensembl
Innerchr14:104256711..104345583hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3888873
hg1988873
hg1888873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834450
Samples
Known GenesADSSL1, AKT1, INF2, SIVA1, ZBTB42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566069
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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