A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566268



Internal ID16353677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105475240..105487998hg38UCSC Ensembl
Innerchr14:105941577..105954335hg19UCSC Ensembl
Innerchr14:105012622..105025380hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3812759
hg1912759
hg1812759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3999n54
Supporting Variantsnssv834936, nssv834934, nssv834935
Samples
Known GenesCRIP1, CRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566268
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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