A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012870



Internal ID19102087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24337..66756hg38UCSC Ensembl
Innerchr3:66011..108439hg19UCSC Ensembl
Innerchr3:41011..83439hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3842420
hg1942429
hg1842429
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4602n100
Supporting Variantsnssv3590223, nssv3590224, nssv3590221, nssv3590222
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)nsv1012870
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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