A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009391



Internal ID19098609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:79555293..79986748hg38UCSC Ensembl
Innerchr3:79604443..80035898hg19UCSC Ensembl
Innerchr3:79687133..80118588hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38431456
hg19431456
hg18431456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596226
Samples
Known GenesROBO1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009391
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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