A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600670



Internal ID16041393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180620412..180636743hg38UCSC Ensembl
Innerchr5:180047412..180063743hg19UCSC Ensembl
Innerchr5:179980018..179996349hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3816332
hg1916332
hg1816332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1047034
Samples
Known GenesFLT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600670
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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