A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008564



Internal ID19097781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:105835736..105924588hg38UCSC Ensembl
Innerchr3:105554580..105643435hg19UCSC Ensembl
Innerchr3:107037270..107126125hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3888853
hg1988856
hg1888856
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4833n100
Supporting Variantsnssv3604392
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)nsv1008564
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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