A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590080



Internal ID16377489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37940970..37943796hg38UCSC Ensembl
Innerchr3:37982461..37985287hg19UCSC Ensembl
Innerchr3:37957465..37960291hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382827
hg192827
hg182827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8284n54
Supporting Variantsnssv962208, nssv962207, nssv962206, nssv962209
Samples
Known GenesCTDSPL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590080
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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