A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999687



Internal ID19159223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:79612987..79689088hg38UCSC Ensembl
Innerchr3:79662137..79738238hg19UCSC Ensembl
Innerchr3:79744827..79820928hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3876102
hg1976102
hg1876102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596227
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)nsv999687
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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