A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590291



Internal ID16377700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52055873..52056728hg38UCSC Ensembl
Innerchr3:52089889..52090744hg19UCSC Ensembl
Innerchr3:52064929..52065784hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38856
hg19856
hg18856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8323n54
Supporting Variantsnssv963078
Samples
Known GenesDUSP7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590291
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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