A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591770



Internal ID16379179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:132013576..132024643hg38UCSC Ensembl
Innerchr3:131732420..131743487hg19UCSC Ensembl
Innerchr3:133215110..133226177hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3811068
hg1911068
hg1811068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv973972
Samples
Known GenesCPNE4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591770
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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