A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600327



Internal ID16387736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:174737213..174769623hg38UCSC Ensembl
Innerchr5:174164216..174196626hg19UCSC Ensembl
Innerchr5:174096822..174129232hg18UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3832411
hg1932411
hg1832411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1045666
Samples
Known GenesMIR4634
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600327
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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