A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012117



Internal ID19101335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:106344377..106430719hg38UCSC Ensembl
Innerchr3:106063224..106149566hg19UCSC Ensembl
Innerchr3:107545914..107632256hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3886343
hg1986343
hg1886343
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604395
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012117
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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