A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002279



Internal ID19091496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162343991..162438955hg38UCSC Ensembl
Innerchr3:162061779..162156743hg19UCSC Ensembl
Innerchr3:163544473..163639437hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3894965
hg1994965
hg1894965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3607947
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)nsv1002279
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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