A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589698



Internal ID16377107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11988560..12026985hg38UCSC Ensembl
Innerchr3:12030034..12068485hg19UCSC Ensembl
Innerchr3:12005034..12043485hg18UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3838426
hg1938452
hg1838452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151872
Samples1780862197_A
Known GenesSYN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589698
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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