A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008449



Internal ID18750980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:105120..189764hg38UCSC Ensembl
Innerchr3:146803..231447hg19UCSC Ensembl
Innerchr3:121803..206447hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3884645
hg1984645
hg1884645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590264
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)nsv1008449
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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