A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592607



Internal ID16380016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176141216..176189554hg38UCSC Ensembl
Innerchr3:175859004..175907342hg19UCSC Ensembl
Innerchr3:177341698..177390036hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3848339
hg1948339
hg1848339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8748n54
Supporting Variantsnssv981611
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592607
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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