A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590079



Internal ID16377488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37940970..37943418hg38UCSC Ensembl
Innerchr3:37982461..37984909hg19UCSC Ensembl
Innerchr3:37957465..37959913hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382449
hg192449
hg182449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8284n54
Supporting Variantsnssv962204, nssv962205
Samples
Known GenesCTDSPL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590079
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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