A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009106



Internal ID19098324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:165541222..165579849hg38UCSC Ensembl
Innerchr3:165259010..165297637hg19UCSC Ensembl
Innerchr3:166741704..166780331hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3838628
hg1938628
hg1838628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4973n100
Supporting Variantsnssv3612583, nssv3612582
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009106
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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