A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566062



Internal ID16006785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104687768..104793397hg38UCSC Ensembl
Innerchr14:105154105..105259734hg19UCSC Ensembl
Innerchr14:104225150..104330779hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38105630
hg19105630
hg18105630
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148716, nssv834443
SamplesHGDP00950
Known GenesADSSL1, AKT1, INF2, SIVA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566062
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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