A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000721



Internal ID18743252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..99533hg38UCSC Ensembl
Innerchr3:60333..141216hg19UCSC Ensembl
Innerchr3:35333..116216hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3880879
hg1980884
hg1880884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4605n100
Supporting Variantsnssv3593530
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)nsv1000721
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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