A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566225



Internal ID16353634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474172..105475136hg38UCSC Ensembl
Innerchr14:105940509..105941473hg19UCSC Ensembl
Innerchr14:105011554..105012518hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38965
hg19965
hg18965
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3992n54
Supporting Variantsnssv834834, nssv834833, nssv834832, nssv834835
Samples
Known GenesCRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566225
Frequency
Sample Size17421
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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