A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008876



Internal ID19098094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:105835736..105926526hg38UCSC Ensembl
Innerchr3:105554580..105645373hg19UCSC Ensembl
Innerchr3:107037270..107128063hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3890791
hg1990794
hg1890794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4833n100
Supporting Variantsnssv3604393
Samples
Known GenesCBLB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008876
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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