A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004219



Internal ID18746750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..104362hg38UCSC Ensembl
Innerchr3:60333..146045hg19UCSC Ensembl
Innerchr3:35333..121045hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3885708
hg1985713
hg1885713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4605n100
Supporting Variantsnssv3590189
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)nsv1004219
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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