A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590356



Internal ID16377765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:53100082..53136484hg38UCSC Ensembl
Innerchr3:53134098..53170500hg19UCSC Ensembl
Innerchr3:53109138..53145540hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3836403
hg1936403
hg1836403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963358
Samples
Known GenesRFT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590356
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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