A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008805



Internal ID18751336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:9694224..9756456hg38UCSC Ensembl
Innerchr3:9735908..9798140hg19UCSC Ensembl
Innerchr3:9710908..9773140hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3862233
hg1962233
hg1862233
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739635
Samples
Known GenesBRPF1, CPNE9, MTMR14, OGG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008805
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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