A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012417



Internal ID19101634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162469014..162498845hg38UCSC Ensembl
Innerchr3:162186802..162216633hg19UCSC Ensembl
Innerchr3:163669496..163699327hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3829832
hg1929832
hg1829832
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3607953
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)nsv1012417
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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