A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012489



Internal ID18755022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4099559..4163939hg38UCSC Ensembl
Innerchr3:4141243..4205623hg19UCSC Ensembl
Innerchr3:4116243..4180623hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3864381
hg1964381
hg1864381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4651n100
Supporting Variantsnssv3590463, nssv3590462
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)nsv1012489
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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