A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592653



Internal ID16380062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:182191149..182245601hg38UCSC Ensembl
Innerchr3:181908937..181963389hg19UCSC Ensembl
Innerchr3:183391631..183446083hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3854453
hg1954453
hg1854453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152555
Samples1780854537_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592653
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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