A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592608



Internal ID16380017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176141216..176197346hg38UCSC Ensembl
Innerchr3:175859004..175915134hg19UCSC Ensembl
Innerchr3:177341698..177397828hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3856131
hg1956131
hg1856131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8748n54
Supporting Variantsnssv981612
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592608
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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