A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566238



Internal ID16353647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474277..105475033hg38UCSC Ensembl
Innerchr14:105940614..105941370hg19UCSC Ensembl
Innerchr14:105011659..105012415hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38757
hg19757
hg18757
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3992n54
Supporting Variantsnssv834881, nssv834879, nssv834880
Samples
Known GenesCRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566238
Frequency
Sample Size17421
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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