A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590446



Internal ID16377855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62972231..63035111hg38UCSC Ensembl
Innerchr3:62957906..63020787hg19UCSC Ensembl
Innerchr3:62932946..62995827hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3862881
hg1962882
hg1862882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963558
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590446
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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